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- [21] LMNB1-Related Adult-Onset Autosomal Dominant Leukodystrophy Presenting as Movement Disorder: A Case Report and Review of the LiteratureFRONTIERS IN NEUROSCIENCE, 2019, 13Zhang, Yanyan论文数: 0 引用数: 0 h-index: 0机构: Zhengzhou Univ, Affiliated Hosp 1, Dept Neurol, Zhengzhou, Henan, Peoples R China Zhengzhou Univ, Affiliated Hosp 1, Dept Neurol, Zhengzhou, Henan, Peoples R ChinaLi, Jie论文数: 0 引用数: 0 h-index: 0机构: Zhengzhou Univ, Affiliated Hosp 1, Dept Neurol, Zhengzhou, Henan, Peoples R China Zhengzhou Univ, Affiliated Hosp 1, Dept Neurol, Zhengzhou, Henan, Peoples R ChinaBai, Rong论文数: 0 引用数: 0 h-index: 0机构: Zhengzhou Univ, Affiliated Hosp 1, Dept Neurol, Zhengzhou, Henan, Peoples R China Zhengzhou Univ, Affiliated Hosp 1, Dept Neurol, Zhengzhou, Henan, Peoples R ChinaWang, Jianping论文数: 0 引用数: 0 h-index: 0机构: Zhengzhou Univ, Affiliated Hosp 1, Dept Neurol, Zhengzhou, Henan, Peoples R China Zhengzhou Univ, Affiliated Hosp 1, Dept Neurol, Zhengzhou, Henan, Peoples R ChinaPeng, Tao论文数: 0 引用数: 0 h-index: 0机构: Zhengzhou Univ, Affiliated Hosp 1, Dept Neurol, Zhengzhou, Henan, Peoples R China Zhengzhou Univ, Affiliated Hosp 1, Dept Neurol, Zhengzhou, Henan, Peoples R ChinaChen, Lijie论文数: 0 引用数: 0 h-index: 0机构: Zhengzhou Univ, Affiliated Hosp 1, Dept Neurol, Zhengzhou, Henan, Peoples R China Zhengzhou Univ, Affiliated Hosp 1, Dept Neurol, Zhengzhou, Henan, Peoples R ChinaWang, Jingtao论文数: 0 引用数: 0 h-index: 0机构: Zhengzhou Univ, Affiliated Hosp 1, Dept Neurol, Zhengzhou, Henan, Peoples R China Zhengzhou Univ, Affiliated Hosp 1, Dept Neurol, Zhengzhou, Henan, Peoples R ChinaLiu, Yanru论文数: 0 引用数: 0 h-index: 0机构: Zhengzhou Univ, Affiliated Hosp 1, Dept Neurol, Zhengzhou, Henan, Peoples R China Zhengzhou Univ, Affiliated Hosp 1, Dept Neurol, Zhengzhou, Henan, Peoples R ChinaTian, Tian论文数: 0 引用数: 0 h-index: 0机构: Zhengzhou Univ, Affiliated Hosp 1, Dept Neurol, Zhengzhou, Henan, Peoples R China Zhengzhou Univ, Affiliated Hosp 1, Dept Neurol, Zhengzhou, Henan, Peoples R ChinaLu, Hong论文数: 0 引用数: 0 h-index: 0机构: Zhengzhou Univ, Affiliated Hosp 1, Dept Neurol, Zhengzhou, Henan, Peoples R China Zhengzhou Univ, Affiliated Hosp 1, Dept Neurol, Zhengzhou, Henan, Peoples R China
- [22] Novel GLDC Compound Heterozygous Variant Leading to Nonketotic Hyperglycinemia: Case Report and Literature ReviewFRONTIERS IN PEDIATRICS, 2021, 9Cao, Yanyan论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Hebei Prov, Inst Pediat Res, Shijiazhuang, Hebei, Peoples R China Childrens Hosp Hebei Prov, Inst Pediat Res, Shijiazhuang, Hebei, Peoples R ChinaMeng, Lingzhi论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Hebei Prov, Dept Neonatol, Shijiazhuang, Hebei, Peoples R China Childrens Hosp Hebei Prov, Inst Pediat Res, Shijiazhuang, Hebei, Peoples R ChinaZhang, Yudong论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Hebei Prov, Dept Neonatol, Shijiazhuang, Hebei, Peoples R China Childrens Hosp Hebei Prov, Inst Pediat Res, Shijiazhuang, Hebei, Peoples R ChinaJiao, Jiancheng论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Hebei Prov, Dept Neonatol, Shijiazhuang, Hebei, Peoples R China Childrens Hosp Hebei Prov, Inst Pediat Res, Shijiazhuang, Hebei, Peoples R ChinaPu, Weicong论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Hebei Prov, Dept Neonatol, Shijiazhuang, Hebei, Peoples R China Childrens Hosp Hebei Prov, Inst Pediat Res, Shijiazhuang, Hebei, Peoples R ChinaMa, Li论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Hebei Prov, Dept Neonatol, Shijiazhuang, Hebei, Peoples R China Childrens Hosp Hebei Prov, Inst Pediat Res, Shijiazhuang, Hebei, Peoples R China
- [23] Compound heterozygous protein C deficiency with pulmonary embolism caused by a novel PROC gene mutation: Case report and literature reviewMEDICINE, 2022, 101 (42) : E31221Zhang, Zhaorui论文数: 0 引用数: 0 h-index: 0机构: Chinese Peoples Liberat Army Gen Hosp, Dept Respirat, Med Ctr 8, Beijing, Peoples R China Chinese Peoples Liberat Army Gen Hosp, Dept Respirat, Med Ctr 8, Beijing, Peoples R ChinaYang, Zhen论文数: 0 引用数: 0 h-index: 0机构: Chinese Peoples Liberat Army Gen Hosp, Dept Respirat, Med Ctr 8, Beijing, Peoples R China Chinese Peoples Liberat Army Gen Hosp, Dept Respirat, Med Ctr 8, Beijing, Peoples R ChinaChen, Mei论文数: 0 引用数: 0 h-index: 0机构: Kingmed Diagnost Grp Co Ltd, Guangzhou, Guangdong, Peoples R China Chinese Peoples Liberat Army Gen Hosp, Dept Respirat, Med Ctr 8, Beijing, Peoples R ChinaLi, Yuzhu论文数: 0 引用数: 0 h-index: 0机构: Chinese Peoples Liberat Army Gen Hosp, Dept Resp Dis, Hainan Hosp, Sanya, Hainan, Peoples R China Chinese Peoples Liberat Army Gen Hosp, Dept Respirat, Med Ctr 8, Beijing, Peoples R China
- [24] A Chinese newborn with Zellweger syndrome and compound heterozygous mutations novel in the PEX1 gene: a case report and literature reviewTRANSLATIONAL PEDIATRICS, 2021, 10 (02) : 446 - 453Lu, Pei论文数: 0 引用数: 0 h-index: 0机构: Shanghai Jiao Tong Univ, Shanghai Childrens Hosp, Dept Neonatol, 355 Luding Rd, Shanghai 200062, Peoples R China Shanghai Jiao Tong Univ, Shanghai Childrens Hosp, Dept Neonatol, 355 Luding Rd, Shanghai 200062, Peoples R ChinaMa, Li论文数: 0 引用数: 0 h-index: 0机构: Shanghai Jiao Tong Univ, Shanghai Childrens Hosp, Dept Neonatol, 355 Luding Rd, Shanghai 200062, Peoples R China Shanghai Jiao Tong Univ, Shanghai Childrens Hosp, Dept Neonatol, 355 Luding Rd, Shanghai 200062, Peoples R ChinaSun, Jingjing论文数: 0 引用数: 0 h-index: 0机构: Shanghai Jiao Tong Univ, Shanghai Childrens Hosp, Dept Neonatol, 355 Luding Rd, Shanghai 200062, Peoples R China Shanghai Jiao Tong Univ, Shanghai Childrens Hosp, Dept Neonatol, 355 Luding Rd, Shanghai 200062, Peoples R ChinaGong, Xiaohui论文数: 0 引用数: 0 h-index: 0机构: Shanghai Jiao Tong Univ, Shanghai Childrens Hosp, Dept Neonatol, 355 Luding Rd, Shanghai 200062, Peoples R China Shanghai Jiao Tong Univ, Shanghai Childrens Hosp, Dept Neonatol, 355 Luding Rd, Shanghai 200062, Peoples R ChinaCai, Cheng论文数: 0 引用数: 0 h-index: 0机构: Shanghai Jiao Tong Univ, Shanghai Childrens Hosp, Dept Neonatol, 355 Luding Rd, Shanghai 200062, Peoples R China Shanghai Jiao Tong Univ, Shanghai Childrens Hosp, Dept Neonatol, 355 Luding Rd, Shanghai 200062, Peoples R China
- [25] Identification of a Compound Heterozygous LMF1 Variants in a Patient with Severe Hypertriglyceridemia - Case Report and Literature ReviewJOURNAL OF ATHEROSCLEROSIS AND THROMBOSIS, 2024, 31 (07) : 1106 - 1111Cao, Conghui论文数: 0 引用数: 0 h-index: 0机构: First Hosp China Med Univ, Inst Endocrinol, Dept Endocrinol & Metab, NHC Key Lab Diag & Treatment Thyroid Dis, Shenyang, Liaoning, Peoples R China First Hosp China Med Univ, Inst Endocrinol, Dept Endocrinol & Metab, NHC Key Lab Diag & Treatment Thyroid Dis, Shenyang, Liaoning, Peoples R ChinaLiu, Yuqi论文数: 0 引用数: 0 h-index: 0机构: First Hosp China Med Univ, Inst Endocrinol, Dept Endocrinol & Metab, NHC Key Lab Diag & Treatment Thyroid Dis, Shenyang, Liaoning, Peoples R China First Hosp China Med Univ, Inst Endocrinol, Dept Endocrinol & Metab, NHC Key Lab Diag & Treatment Thyroid Dis, Shenyang, Liaoning, Peoples R ChinaLiu, Lu论文数: 0 引用数: 0 h-index: 0机构: First Hosp China Med Univ, Inst Endocrinol, Dept Endocrinol & Metab, NHC Key Lab Diag & Treatment Thyroid Dis, Shenyang, Liaoning, Peoples R China First Hosp China Med Univ, Inst Endocrinol, Dept Endocrinol & Metab, NHC Key Lab Diag & Treatment Thyroid Dis, Shenyang, Liaoning, Peoples R ChinaWang, Xiaoli论文数: 0 引用数: 0 h-index: 0机构: First Hosp China Med Univ, Inst Endocrinol, Dept Endocrinol & Metab, NHC Key Lab Diag & Treatment Thyroid Dis, Shenyang, Liaoning, Peoples R China First Hosp China Med Univ, Inst Endocrinol, Dept Endocrinol & Metab, NHC Key Lab Diag & Treatment Thyroid Dis, Shenyang, Liaoning, Peoples R China
- [26] Renal hypouricemia caused by novel compound heterozygous mutations in the SLC22A12 gene: a case report with literature reviewBMC MEDICAL GENETICS, 2018, 19Zhou, Zhaowei论文数: 0 引用数: 0 h-index: 0机构: Shanghai Jiao Tong Univ, BioX Inst, Key Lab Genet Dev & Neuropsychiat Disorders, Minist Educ, 1954 Huashan Rd, Shanghai 200030, Peoples R China Shanghai Jiao Tong Univ, BioX Inst, Key Lab Genet Dev & Neuropsychiat Disorders, Minist Educ, 1954 Huashan Rd, Shanghai 200030, Peoples R ChinaMa, Lidan论文数: 0 引用数: 0 h-index: 0机构: Shandong Gout Clin Med Ctr, Qingdao 266003, Peoples R China Qingdao Univ, Shandong Prov Key Lab Metab Dis, Affiliated Hosp, 16 Jiangsu Rd, Qingdao 266003, Peoples R China Qingdao Univ, Affiliated Hosp, Dept Endocrinol & Metab, Qingdao 266003, Peoples R China Shanghai Jiao Tong Univ, BioX Inst, Key Lab Genet Dev & Neuropsychiat Disorders, Minist Educ, 1954 Huashan Rd, Shanghai 200030, Peoples R ChinaZhou, Juan论文数: 0 引用数: 0 h-index: 0机构: Shanghai Jiao Tong Univ, BioX Inst, Key Lab Genet Dev & Neuropsychiat Disorders, Minist Educ, 1954 Huashan Rd, Shanghai 200030, Peoples R China Shanghai Jiao Tong Univ, BioX Inst, Key Lab Genet Dev & Neuropsychiat Disorders, Minist Educ, 1954 Huashan Rd, Shanghai 200030, Peoples R ChinaSong, Zhijian论文数: 0 引用数: 0 h-index: 0机构: Shanghai Jiao Tong Univ, BioX Inst, Key Lab Genet Dev & Neuropsychiat Disorders, Minist Educ, 1954 Huashan Rd, Shanghai 200030, Peoples R China Shanghai Jiao Tong Univ, BioX Inst, Key Lab Genet Dev & Neuropsychiat Disorders, Minist Educ, 1954 Huashan Rd, Shanghai 200030, Peoples R ChinaZhang, Jinmai论文数: 0 引用数: 0 h-index: 0机构: Shanghai Jiao Tong Univ, BioX Inst, Key Lab Genet Dev & Neuropsychiat Disorders, Minist Educ, 1954 Huashan Rd, Shanghai 200030, Peoples R China Shanghai Jiao Tong Univ, BioX Inst, Key Lab Genet Dev & Neuropsychiat Disorders, Minist Educ, 1954 Huashan Rd, Shanghai 200030, Peoples R ChinaWang, Ke论文数: 0 引用数: 0 h-index: 0机构: Shanghai Jiao Tong Univ, BioX Inst, Key Lab Genet Dev & Neuropsychiat Disorders, Minist Educ, 1954 Huashan Rd, Shanghai 200030, Peoples R China Shanghai Jiao Tong Univ, BioX Inst, Key Lab Genet Dev & Neuropsychiat Disorders, Minist Educ, 1954 Huashan Rd, Shanghai 200030, Peoples R ChinaChen, Boyu论文数: 0 引用数: 0 h-index: 0机构: Shanghai Jiao Tong Univ, BioX Inst, Key Lab Genet Dev & Neuropsychiat Disorders, Minist Educ, 1954 Huashan Rd, Shanghai 200030, Peoples R China Shanghai Jiao Tong Univ, BioX Inst, Key Lab Genet Dev & Neuropsychiat Disorders, Minist Educ, 1954 Huashan Rd, Shanghai 200030, Peoples R ChinaPan, Dun论文数: 0 引用数: 0 h-index: 0机构: Shanghai Jiao Tong Univ, BioX Inst, Key Lab Genet Dev & Neuropsychiat Disorders, Minist Educ, 1954 Huashan Rd, Shanghai 200030, Peoples R China Shanghai Jiao Tong Univ, BioX Inst, Key Lab Genet Dev & Neuropsychiat Disorders, Minist Educ, 1954 Huashan Rd, Shanghai 200030, Peoples R ChinaLi, Zhiqiang论文数: 0 引用数: 0 h-index: 0机构: Shanghai Jiao Tong Univ, BioX Inst, Key Lab Genet Dev & Neuropsychiat Disorders, Minist Educ, 1954 Huashan Rd, Shanghai 200030, Peoples R China Qingdao Univ, SJTU BioX Inst, Qingdao Branch, Biomed Sci Inst, Qingdao 266003, Peoples R China Shanghai Jiao Tong Univ, BioX Inst, Key Lab Genet Dev & Neuropsychiat Disorders, Minist Educ, 1954 Huashan Rd, Shanghai 200030, Peoples R ChinaLi, Changgui论文数: 0 引用数: 0 h-index: 0机构: Shandong Gout Clin Med Ctr, Qingdao 266003, Peoples R China Qingdao Univ, Shandong Prov Key Lab Metab Dis, Affiliated Hosp, 16 Jiangsu Rd, Qingdao 266003, Peoples R China Qingdao Univ, Affiliated Hosp, Dept Endocrinol & Metab, Qingdao 266003, Peoples R China Qingdao Univ, Metab Dis Inst, Qingdao 266003, Peoples R China Shanghai Jiao Tong Univ, BioX Inst, Key Lab Genet Dev & Neuropsychiat Disorders, Minist Educ, 1954 Huashan Rd, Shanghai 200030, Peoples R ChinaShi, Yongyong论文数: 0 引用数: 0 h-index: 0机构: Shanghai Jiao Tong Univ, BioX Inst, Key Lab Genet Dev & Neuropsychiat Disorders, Minist Educ, 1954 Huashan Rd, Shanghai 200030, Peoples R China Shandong Gout Clin Med Ctr, Qingdao 266003, Peoples R China Qingdao Univ, Shandong Prov Key Lab Metab Dis, Affiliated Hosp, 16 Jiangsu Rd, Qingdao 266003, Peoples R China Qingdao Univ, SJTU BioX Inst, Qingdao Branch, Biomed Sci Inst, Qingdao 266003, Peoples R China Shanghai Jiao Tong Univ, BioX Inst, Key Lab Genet Dev & Neuropsychiat Disorders, Minist Educ, 1954 Huashan Rd, Shanghai 200030, Peoples R China
- [27] Novel compound heterozygous mutations of the NPC1 gene associated with Niemann-pick disease type C: a case report and review of the literatureBMC Infectious Diseases, 24Chaoxin Tao论文数: 0 引用数: 0 h-index: 0机构: Shijiazhuang Ping’an Hospital,Department of Internal MedicineMin Zhao论文数: 0 引用数: 0 h-index: 0机构: Shijiazhuang Ping’an Hospital,Department of Internal MedicineXiaohui Zhang论文数: 0 引用数: 0 h-index: 0机构: Shijiazhuang Ping’an Hospital,Department of Internal MedicineJihong Hao论文数: 0 引用数: 0 h-index: 0机构: Shijiazhuang Ping’an Hospital,Department of Internal MedicineQiuyue Huo论文数: 0 引用数: 0 h-index: 0机构: Shijiazhuang Ping’an Hospital,Department of Internal MedicineJie Sun论文数: 0 引用数: 0 h-index: 0机构: Shijiazhuang Ping’an Hospital,Department of Internal MedicineJiangtao Xing论文数: 0 引用数: 0 h-index: 0机构: Shijiazhuang Ping’an Hospital,Department of Internal MedicineYuna Zhang论文数: 0 引用数: 0 h-index: 0机构: Shijiazhuang Ping’an Hospital,Department of Internal MedicineJianhong Zhao论文数: 0 引用数: 0 h-index: 0机构: Shijiazhuang Ping’an Hospital,Department of Internal MedicineHuaipeng Huang论文数: 0 引用数: 0 h-index: 0机构: Shijiazhuang Ping’an Hospital,Department of Internal Medicine
- [28] Compound heterozygous variants in PGAP1 causing severe psychomotor retardation, brain atrophy, recurrent apneas and delayed myelination: a case report and literature reviewBMC NEUROLOGY, 2016, 16Kettwig, Matthias论文数: 0 引用数: 0 h-index: 0机构: Univ Gottingen, Univ Med Ctr, Dept Pediat & Pediat Neurol, D-37075 Gottingen, Germany Univ Gottingen, Univ Med Ctr, Dept Pediat & Pediat Neurol, D-37075 Gottingen, GermanyElpeleg, Orly论文数: 0 引用数: 0 h-index: 0机构: Hadassah Hebrew Univ Med Ctr, Monique & Jacques Roboh Dept Genet Res, Jerusalem, Israel Univ Gottingen, Univ Med Ctr, Dept Pediat & Pediat Neurol, D-37075 Gottingen, GermanyWegener, Eike论文数: 0 引用数: 0 h-index: 0机构: Univ Gottingen, Univ Med Ctr, Dept Pediat & Pediat Neurol, D-37075 Gottingen, Germany Univ Gottingen, Univ Med Ctr, Dept Pediat & Pediat Neurol, D-37075 Gottingen, GermanyDreha-Kulaczewski, Steffi论文数: 0 引用数: 0 h-index: 0机构: Univ Gottingen, Univ Med Ctr, Dept Pediat & Pediat Neurol, D-37075 Gottingen, Germany Univ Gottingen, Univ Med Ctr, Dept Pediat & Pediat Neurol, D-37075 Gottingen, GermanyHenneke, Marco论文数: 0 引用数: 0 h-index: 0机构: Univ Gottingen, Univ Med Ctr, Dept Pediat & Pediat Neurol, D-37075 Gottingen, Germany Univ Gottingen, Univ Med Ctr, Dept Pediat & Pediat Neurol, D-37075 Gottingen, GermanyGaertner, Jutta论文数: 0 引用数: 0 h-index: 0机构: Univ Gottingen, Univ Med Ctr, Dept Pediat & Pediat Neurol, D-37075 Gottingen, Germany Univ Gottingen, Univ Med Ctr, Dept Pediat & Pediat Neurol, D-37075 Gottingen, GermanyHuppke, Peter论文数: 0 引用数: 0 h-index: 0机构: Univ Gottingen, Univ Med Ctr, Dept Pediat & Pediat Neurol, D-37075 Gottingen, Germany Univ Gottingen, Univ Med Ctr, Dept Pediat & Pediat Neurol, D-37075 Gottingen, Germany
- [29] Novel Frameshift Heterozygous Mutation in UBAP1 Gene Causing Spastic Paraplegia-80: Case Report With Literature ReviewFRONTIERS IN NEUROLOGY, 2022, 13Zhang, Chao论文数: 0 引用数: 0 h-index: 0机构: Anhui Med Univ, Suzhou Hosp, Suzhou Municipal Hosp, Suzhou, Anhui Province, Peoples R China Shanghai Jiao Tong Univ Affiliated Sixth Peoples H, Dept Neurol, Shanghai, Peoples R China Anhui Med Univ, Suzhou Hosp, Suzhou Municipal Hosp, Suzhou, Anhui Province, Peoples R ChinaZhu, Xiaowei论文数: 0 引用数: 0 h-index: 0机构: Anhui Med Univ, Suzhou Hosp, Suzhou Municipal Hosp, Suzhou, Anhui Province, Peoples R China Shanghai Jiao Tong Univ Affiliated Sixth Peoples H, Dept Neurol, Shanghai, Peoples R China Anhui Med Univ, Suzhou Hosp, Suzhou Municipal Hosp, Suzhou, Anhui Province, Peoples R ChinaZhu, Zeyu论文数: 0 引用数: 0 h-index: 0机构: Shanghai Jiao Tong Univ Affiliated Sixth Peoples H, Dept Neurol, Shanghai, Peoples R China Anhui Med Univ, Suzhou Hosp, Suzhou Municipal Hosp, Suzhou, Anhui Province, Peoples R ChinaNi, Ruilong论文数: 0 引用数: 0 h-index: 0机构: Shanghai Jiao Tong Univ Affiliated Sixth Peoples H, Dept Neurol, Shanghai, Peoples R China Anhui Univ Sci & Technol, Sch Med, Huainan, Peoples R China Anhui Med Univ, Suzhou Hosp, Suzhou Municipal Hosp, Suzhou, Anhui Province, Peoples R ChinaLiu, Taotao论文数: 0 引用数: 0 h-index: 0机构: Shanghai Jiao Tong Univ Affiliated Sixth Peoples H, Dept Neurol, Shanghai, Peoples R China Anhui Univ Sci & Technol, Sch Med, Huainan, Peoples R China Anhui Med Univ, Suzhou Hosp, Suzhou Municipal Hosp, Suzhou, Anhui Province, Peoples R ChinaZheng, Haoran论文数: 0 引用数: 0 h-index: 0机构: Shanghai Jiao Tong Univ Affiliated Sixth Peoples H, Dept Neurol, Shanghai, Peoples R China Anhui Univ Sci & Technol, Sch Med, Huainan, Peoples R China Anhui Med Univ, Suzhou Hosp, Suzhou Municipal Hosp, Suzhou, Anhui Province, Peoples R ChinaLiu, Shihua论文数: 0 引用数: 0 h-index: 0机构: Anhui Med Univ, Suzhou Hosp, Suzhou Municipal Hosp, Suzhou, Anhui Province, Peoples R China Anhui Med Univ, Suzhou Hosp, Suzhou Municipal Hosp, Suzhou, Anhui Province, Peoples R ChinaCao, Li论文数: 0 引用数: 0 h-index: 0机构: Anhui Med Univ, Suzhou Hosp, Suzhou Municipal Hosp, Suzhou, Anhui Province, Peoples R China Shanghai Jiao Tong Univ Affiliated Sixth Peoples H, Dept Neurol, Shanghai, Peoples R China Anhui Med Univ, Suzhou Hosp, Suzhou Municipal Hosp, Suzhou, Anhui Province, Peoples R ChinaZhong, Ping论文数: 0 引用数: 0 h-index: 0机构: Anhui Med Univ, Suzhou Hosp, Suzhou Municipal Hosp, Suzhou, Anhui Province, Peoples R China Anhui Med Univ, Suzhou Hosp, Suzhou Municipal Hosp, Suzhou, Anhui Province, Peoples R ChinaTian, Wotu论文数: 0 引用数: 0 h-index: 0机构: Shanghai Jiao Tong Univ Affiliated Sixth Peoples H, Dept Neurol, Shanghai, Peoples R China Anhui Med Univ, Suzhou Hosp, Suzhou Municipal Hosp, Suzhou, Anhui Province, Peoples R China
- [30] Compound heterozygous variants in PGAP1 causing severe psychomotor retardation, brain atrophy, recurrent apneas and delayed myelination: a case report and literature reviewBMC Neurology, 16Matthias Kettwig论文数: 0 引用数: 0 h-index: 0机构: University Medical Center,Department of Pediatrics and Pediatric NeurologyOrly Elpeleg论文数: 0 引用数: 0 h-index: 0机构: University Medical Center,Department of Pediatrics and Pediatric NeurologyEike Wegener论文数: 0 引用数: 0 h-index: 0机构: University Medical Center,Department of Pediatrics and Pediatric NeurologySteffi Dreha-Kulaczewski论文数: 0 引用数: 0 h-index: 0机构: University Medical Center,Department of Pediatrics and Pediatric NeurologyMarco Henneke论文数: 0 引用数: 0 h-index: 0机构: University Medical Center,Department of Pediatrics and Pediatric NeurologyJutta Gärtner论文数: 0 引用数: 0 h-index: 0机构: University Medical Center,Department of Pediatrics and Pediatric NeurologyPeter Huppke论文数: 0 引用数: 0 h-index: 0机构: University Medical Center,Department of Pediatrics and Pediatric Neurology