A Novel Mutation in the Espin Gene Causes Autosomal Recessive Nonsyndromic Hearing Loss But No Apparent Vestibular Dysfunction in a Moroccan Family

被引：13

作者：

Boulouiz, Redouane ^{[1
,2
]}

Li, Yun ^{[3
,4
]}

Soualhine, Hafid ^{[1
]}

Abidi, Omar ^{[1
,2
]}

Chafik, Abdelaziz ^{[2
]}

Nuernberg, Gudrun ^{[5
]}

Becker, Christian ^{[5
]}

Nuernberg, Peter ^{[5
,6
]}

Kubisch, Christian ^{[3
,4
,6
]}

Wollnik, Bernd ^{[3
]}

Barakat, Abdelhamid ^{[1
]}

机构：

[1] Inst Pasteur, Dept Genet, Casablanca, Morocco

[2] Univ Chouaib Doukkali, Fac Sci, El Jadida, Morocco

[3] Univ Cologne, CMMC, Cologne, Germany

[4] Univ Cologne, Inst Human Genet, Cologne, Germany

[5] Univ Cologne, Cologne Ctr Genom, Cologne, Germany

[6] Univ Cologne, Inst Genet, D-5000 Cologne, Germany

来源：

AMERICAN JOURNAL OF MEDICAL GENETICS PART A | 2008年 / 146A卷 / 23期

关键词：

D O I：

10.1002/ajmg.a.32525

中图分类号：

Q3 [遗传学];

学科分类号：

071007 [遗传学]; 090102 [作物遗传育种];

摘要：

引用

页码：3086 / 3089

页数：4

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