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

页码：962 / 962

页数：1

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