Analysis of recurrent mutations in different Iranian families with hearing loss

被引：0

作者：

Hofrichter, M. A. H. ^{[1
]}

Rad, A. ^{[2
,3
]}

Kolb, S. ^{[1
]}

Weingart, J. ^{[1
]}

Doll, J. ^{[1
]}

Mueller, T. ^{[4
]}

Remmele, C. ^{[1
,5
]}

Dittrich, M. ^{[1
,4
]}

Maroofian, R. ^{[6
]}

Haaf, T. ^{[1
]}

Vona, B. ^{[1
,3
]}

机构：

[1] Julius Maximilians Univ, Inst Human Genet, Wurzburg, Germany

[2] Sabzevar Univ Med Sci, Cellular & Mol Res Ctr, Sabzevar, Iran

[3] Eberhard Karls Univ Tubingen, Tubingen Hearing Res Ctr THRC, Dept Otorhinolaryngol Head & Neck Surg, Tubingen, Germany

[4] Julius Maximilians Univ, Inst Bioinformat, Wurzburg, Germany

[5] Univ Hosp Wurzburg, Ctr Rare Dis, Wurzburg, Germany

[6] St Georges Univ London, Genet & Mol Cell Sci Res Ctr, Cranmer Terrace, London, England

来源：

EUROPEAN JOURNAL OF HUMAN GENETICS | 2020年 / 28卷 / SUPPL 1期

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：

P02.31.C

引用

页码：193 / 194

页数：2

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