A new locus for nonsyndromic hereditary hearing impairment, DFNA17, maps to chromosome 22 and represents a gene for cochleosaccular degeneration

被引：29

作者：

Lalwani, AK ^{[1
]}

Luxford, WM

Mhatre, AN

Attaie, A

Wilcox, ER

Castelein, CM

机构：

[1] Univ Calif San Francisco, Dept Otolaryngol Head & Neck Surg, Lab Mol Otol, San Francisco, CA 94143 USA

[2] House Ear Clin, Los Angeles, CA USA

[3] Natl Inst Deafness & Other Commun Disorders, Mol Genet Lab, Bethesda, MD USA

来源：

AMERICAN JOURNAL OF HUMAN GENETICS | 1999年 / 64卷 / 01期

关键词：

D O I：

10.1086/302216

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：318 / 323

页数：6

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