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An Extended Iranian Family with Autosomal Dominant Non-syndromic Hearing Loss Associated with A Nonsense Mutation in the DIAPH1 Gene.

Marzieh Mohseni, Yusuf Mohammadi,Farzane Zare Ashrafi,Fatemeh Ghodratpour,Khadijeh Jalalvand,Sanaz Arzhangi,Mojgan Babanejad,Mohammad Hossein Azizi,Kimia Kahrizi,Hossein Najmabadi

ARCHIVES OF IRANIAN MEDICINE（2023）

引用 1|浏览22
关键词
DIAPH1,Exome sequencing,Iran,Non syndromic hearing loss
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