LINKAGE OF A GENE FOR DOMINANT NON-SYNDROMIC DEAFNESS TO CHROMOSOME-19

被引：65

作者：

CHEN, AH

NI, L

FUKUSHIMA, K

MARIETTA, J

ONEILL, M

COUCKE, P

WILLEMS, P

SMITH, RJH

机构：

[1] UNIV IOWA,DEPT DERMATOL,MOLEC OTOLARYNGOL RES LABS,IOWA CITY,IA 52242

[2] UNIV ANTWERP,DEPT MED GENET,B-2020 ANTWERP,BELGIUM

来源：

HUMAN MOLECULAR GENETICS | 1995年 / 4卷 / 06期

关键词：

D O I：

10.1093/hmg/4.6.1073

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：

Inherited hearing impairment can occur either in the presence of other clinical features (syndromic hearing loss, SHL) or in isolation (non-syndromic hearing loss, NSHL), The latter is more common and is highly heterogeneous, To date, six NSHL loci have been mapped, We report the identification of a seventh locus (DFNA4) on chromosome 19q13 and suggest DM kinase as a possible candidate gene.

引用

页码：1073 / 1076

页数：4

共 40 条

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