A novel connexin 26 (GJB2) mutation in a case of sensorineural hearing loss, keratoderma and knuckle pads.

被引：0
|
作者：
Leonard, N
Krol, AL
Hasse, SM
Sprysak, K
Somerville, MJ
机构：
[1] Oregon Hlth Sci Univ, Portland, OR 97201 USA
[2] Univ Alberta, Dept Med Genet, Edmonton, AB, Canada
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：
2198
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收藏
页码：544 / 544
页数：1
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