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Mapping of the otogelin gene (OTGN) to mouse Chromosome 7 and human Chromosome 11p14.3: a candidate for human autosomal recessive nonsyndromic deafness DFNB18

被引：13
作者：
Cohen-Salmon, M
Mattei, MG
Petit, C
机构：
[1] Inst Pasteur, URA 1968, CNRS, Unite Genet Deficits Sensoriels, F-75724 Paris 15, France
[2] INSERM, U406, Fac Med, Unite Genet Med & Dev, F-13385 Marseille, France
来源：
MAMMALIAN GENOME | 1999年 / 10卷 / 05期
关键词：
D O I：
10.1007/s003359901033
中图分类号：
Q5 [生物化学]; Q7 [分子生物学];
学科分类号：
071010 ; 081704 ;
摘要：
[No abstract available]
引用
收藏
页码：520 / 522
页数：3
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