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首页|期刊导航|中华医学杂志(英文版)|A Novel De novo GATA?binding Protein 3 Mutation in a Patient with Hypoparathyroidism, Sensorineural Deafness, and Renal Dysplasia Syndrome

A Novel De novo GATA?binding Protein 3 Mutation in a Patient with Hypoparathyroidism, Sensorineural Deafness, and Renal Dysplasia Syndrome

Xue‑Ying Chu Yue‑Peng Li Min Nie Ou Wang Yan Jiang Mei Li Wei‑Bo Xia Xiao‑Ping Xing

中华医学杂志(英文版)Issue(11):1378-1380,3.
中华医学杂志(英文版)Issue(11):1378-1380,3.DOI:10.4103/0366‑6999.206348

A Novel De novo GATA?binding Protein 3 Mutation in a Patient with Hypoparathyroidism, Sensorineural Deafness, and Renal Dysplasia Syndrome

A Novel De novo GATA?binding Protein 3 Mutation in a Patient with Hypoparathyroidism, Sensorineural Deafness, and Renal Dysplasia Syndrome

Xue‑Ying Chu 1Yue‑Peng Li 1Min Nie 1Ou Wang 1Yan Jiang 1Mei Li 1Wei‑Bo Xia 1Xiao‑Ping Xing1

作者信息

  • 1. Department of Endocrinology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100730, China
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摘要

关键词

De novo Mutation/GATA‑binding Protein 3 Gene/Hypoparathyroidism/Sensorineural Deafness/and Renal Dysplasia Syndrome

Key words

De novo Mutation/GATA‑binding Protein 3 Gene/Hypoparathyroidism/Sensorineural Deafness/and Renal Dysplasia Syndrome

引用本文复制引用

Xue‑Ying Chu,Yue‑Peng Li,Min Nie,Ou Wang,Yan Jiang,Mei Li,Wei‑Bo Xia,Xiao‑Ping Xing..A Novel De novo GATA?binding Protein 3 Mutation in a Patient with Hypoparathyroidism, Sensorineural Deafness, and Renal Dysplasia Syndrome[J].中华医学杂志(英文版),2017,(11):1378-1380,3.

基金项目

This study was supported by grants from the National Natural Science Foundation of China (No. 81270873 and No. 81100559) and the National Key Program of Clinical Science (WBYZ2011?873). (No. 81270873 and No. 81100559)

中华医学杂志(英文版)

OACSCDCSTPCDMEDLINESCI

0366-6999

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