Whole-exome sequencing revealed a novel candidate gene, ARHGAP22, as potential cause of non-syndromic hearing loss in an Iranian family

被引：0
|
作者：
Rezvandeh, Raziye Rezvani [1 ]
Kazemi, Negar [1 ]
Ashrafi, Farzane Zare [1 ,2 ]
Edizadeh, Masoud
Ghodratpour, Fatemeh [1 ]
Keshavarzi, Fatemeh [1 ]
Jalalvand, Khadijeh [1 ]
Arzhangi, Sanaz [1 ]
Kahrizi, Kimia [1 ]
Najmabadi, Hossein [1 ]
Mohseni, Marzieh [1 ]
机构：
[1] Univ Social Welf & Rehabil Sci, Genet Res Ctr, Tehran, Iran
[2] Genoks Genet Diag Ctr, Dept Bioinformat, Ankara, Turkiye
来源：
EUROPEAN JOURNAL OF HUMAN GENETICS | 2024年 / 32卷
关键词：
D O I：
暂无
中图分类号：
Q5 [生物化学]; Q7 [分子生物学];
学科分类号：
071010 ; 081704 ;
摘要：
EP04.013
引用
收藏
页码：962 / 962
页数：1
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