Hearing loss: frequency and, functional studies of the most common CX26 alleles.

被引：0
|
作者：
Gasparini, P
Veronesi, V
Bicego, M
Melchioda, S
Zelante, L
Di Iorio, E
Bruzzone, R
D'Andrea, P
机构：
[1] SUN TIGEM, Med Genet, Naples, Italy
[2] Univ Trieste, Dip Biochim Biofis & Chim Macromol, Trieste, Italy
[3] IRCCS, CSS, Serv Genet Med, San Giovanni Rotondo, Italy
[4] TIGEM, Naples, Italy
[5] Inst Pasteur, Dept Neurosci, Paris, France
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：
2187
引用
收藏
页码：543 / 543
页数：1
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