Novel mutations of connexin 26 (GJB2) in families of non-syndromic recessive hearing loss.

被引：0
|
作者：
Kelley, PM [1 ]
Harris, D [1 ]
Comer, B [1 ]
Smith, SD [1 ]
Kimberling, WJ [1 ]
机构：
[1] Boys Town Natl Res Hosp, Omaha, NE 68131 USA
来源：
AMERICAN JOURNAL OF HUMAN GENETICS | 1997年 / 61卷 / 04期
关键词：
D O I：
暂无
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
1970
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收藏
页码：A336 / A336
页数：1
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