A Chinese Boy with Mowat-Wilson Syndrome Caused by a 10 bp Deletion in the ZEB2 Gene

被引：4
作者：
Wei, Lin [1 ]
Han, Xiao [2 ]
Li, Xue [1 ]
Han, Bingjuan [1 ]
Nie, Wenying [1 ]
机构：
[1] Shandong First Med Univ, Jinan Maternal & Child Care Hosp, Jinan Matern & Child Care Hosp, Jinan 250001, Shandong, Peoples R China
[2] Shandong Univ, Jinan Cent Hosp, Cheeloo Coll Med, Jinan 250012, Shandong, Peoples R China
来源：
PHARMACOGENOMICS & PERSONALIZED MEDICINE | 2021年 / 14卷
关键词：
Mowat-Wilson syndrome; ZEB2; gene mutation; phenotype; SMAD-INTERACTING PROTEIN-1; HIRSCHSPRUNG-DISEASE; MENTAL-RETARDATION; MUTATIONS; PHENOTYPE; FEATURES; ZFHX1B; GENE;
D O I：
10.2147/PGPM.S320128
中图分类号：
R9 [药学];
学科分类号：
1007 ;
摘要：
Mowat-Wilson syndrome, ZEB2, gene mutation, phenotype
引用
收藏
页码：1041 / 1045
页数：5
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