GJB2 mutations in Indian families with Autosomal Recessive Nonsyndromic Sensorineural Hearing Loss (ARNSHL).

被引：0
|
作者：
Vijaya, R
Kabra, M
Menon, PSN
Deka, RC
机构：
[1] All India Inst Med Sci, Dept Otorhinolaryngol, New Delhi, India
[2] All India Inst Med Sci, Dept Pediat, Genet Unit, New Delhi, India
来源：
AMERICAN JOURNAL OF HUMAN GENETICS | 2003年 / 73卷 / 05期
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D O I：
暂无
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
2199
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收藏
页码：544 / 544
页数：1
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