High prevalence of W24X mutation in Indian families with non-syndromic deafness.

被引：0
|
作者：
Vijaya, R
Ghosh, R
Kabra, M
Menon, PSN
Deka, RC
机构：
[1] All India Inst Med Sci, Dept Pediat, Dept Otorhinolaryngol, New Delhi, India
[2] All India Inst Med Sci, Dept Otorhinolaryngol, New Delhi, India
来源：
AMERICAN JOURNAL OF HUMAN GENETICS | 2002年 / 71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：
2000
引用
收藏
页码：511 / 511
页数：1
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