Novel compound heterozygous mutations in SERPINH1 cause rare autosomal recessive osteogenesis imperfecta type X

被引：0

作者：

Y. Song

D. Zhao

X. Xu

F. Lv

L. Li

Y. Jiang

O. Wang

W. Xia

X. Xing

M. Li

机构：

[1] Peking Union Medical College Hospital,Department of Endocrinology, Key Laboratory of Endocrinology, National Health and Family Planning Commission

[2] Chinese Academy of Medical Sciences and Peking Union Medical College,Department of Endocrinology, Beijing Jishuitan Hospital

[3] The Fourth Clinical Medical College of Peking University,undefined

来源：

Osteoporosis International | 2018年 / 29卷

关键词：

Bisphosphonates; HSP47; Osteogenesis imperfecta;

D O I：

暂无

中图分类号：

学科分类号：

摘要：

引用

页码：1389 / 1396

页数：7

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