DFNA49, a novel locus for autosomal dominant non-syndromic hearing loss, maps proximal to DFNA7/DFNM1 region on chromosome 1q21-q23

被引：13
|
作者：
Moreno-Pelayo, MA
Modamio-Hoybjor, S
Mencía, A
del Castillo, I
Chardenoux, S
Fernández-Burriel, M
Lathrop, M
Petit, C
Moreno, F
机构：
[1] Hosp Ramon & Cajal, Unidad Genet Mol, E-28034 Madrid, Spain
[2] Inst Pasteur, Unite Genet Deficits Sensoriels, CNRS, URA 1968, Paris, France
[3] Hosp Univ Materno Infantil, Genet Mol Lab, Las Palmas Gran Canaria, Spain
[4] Ctr Natl Genotypage, Evry, France
来源：
JOURNAL OF MEDICAL GENETICS | 2003年 / 40卷 / 11期
关键词：
D O I：
10.1136/jmg.40.11.832
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
引用
收藏
页码：832 / 836
页数：5
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