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首页|期刊导航|中华医学杂志（英文版）|Clinical Auditory Phenotypes Associated with GATA3 Gene Mutations in Familial Hypoparathyroidism-deafness-renal Dysplasia Syndrome

Clinical Auditory Phenotypes Associated with GATA3 Gene Mutations in Familial Hypoparathyroidism-deafness-renal Dysplasia Syndrome

Li Wang Jin-Long Liang Han-Lin Zhou Huan-Ming Yang Wen-Ping Xiong Qiu-Jing Zhang Da-Yong Wang Qiu-Ju Wang Qiong-Fen Lin Hong-Yang Wang Jing Guan Lan Lan Lin-Yi Xie Lan Yu Ju Yang Cui Zhao

中华医学杂志（英文版）2017，Vol.130Issue(6)：703-709,7.
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中华医学杂志（英文版）2017，Vol.130Issue(6)：703-709,7.DOI:10.4103/0366-6999.201600

Clinical Auditory Phenotypes Associated with GATA3 Gene Mutations in Familial Hypoparathyroidism-deafness-renal Dysplasia Syndrome

Clinical Auditory Phenotypes Associated with GATA3 Gene Mutations in Familial Hypoparathyroidism-deafness-renal Dysplasia Syndrome

Li Wang 1Jin-Long Liang 2Han-Lin Zhou 3Huan-Ming Yang 3Wen-Ping Xiong 3Qiu-Jing Zhang 4Da-Yong Wang 1Qiu-Ju Wang 1Qiong-Fen Lin 1Hong-Yang Wang 1Jing Guan 3Lan Lan 1Lin-Yi Xie 1Lan Yu 1Ju Yang 1Cui Zhao1

作者信息

  • 1. Department of Otolaryngology Head and Neck Surgery, Institute of Otolaryngology, Chinese People's Liberation Army General Hospital,Beijing 100853, China
  • 2. Department of Clinical Medicine, School of Medicine, Nankai University, Tianjin 300071, China
  • 3. Beijing Genomics Institute, Shenzhen, Guangdong 518083, China
  • 4. James D.Watson Institute of Genome Sciences, Hangzhou, Zhejiang 310058, China
  • 折叠

摘要

关键词

GATA binding protein 3/Genetic Anticipation/Hypoparathyroidism-deafness-renal Dysplasia Syndrome

Key words

GATA binding protein 3/Genetic Anticipation/Hypoparathyroidism-deafness-renal Dysplasia Syndrome

引用本文复制引用

Li Wang,Jin-Long Liang,Han-Lin Zhou,Huan-Ming Yang,Wen-Ping Xiong,Qiu-Jing Zhang,Da-Yong Wang,Qiu-Ju Wang,Qiong-Fen Lin,Hong-Yang Wang,Jing Guan,Lan Lan,Lin-Yi Xie,Lan Yu,Ju Yang,Cui Zhao..Clinical Auditory Phenotypes Associated with GATA3 Gene Mutations in Familial Hypoparathyroidism-deafness-renal Dysplasia Syndrome[J].中华医学杂志（英文版）,2017,130(6):703-709,7.

基金项目

This work was supported by grants from the National Natural Science Foundation of China (No.81530032),The National Key Basic Research Program of China(No.2014CB943001),and The China Postdoctoral Science Foundation (No.2015M572766 and No.2015M572690). （No.81530032）

中华医学杂志（英文版）

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0366-6999

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