Contribution of connexin26 (GJB2) mutations and founder effect to non-syndromic hearing loss in India -: art. no. e68
Contribution of connexin26 (GJB2) mutations and founder effect to non-syndromic hearing loss in India -: art. no. e68
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DOI：
10.1136/jmg.40.5.e68
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发表时间：
2003-05-01
影响因子：
4
通讯作者：
Anand, A
中科院分区：
文献类型：
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作者：
RamShankar, M;Girirajan, S;Anand, A
方法招募独立确定的先证者（n= 215）进行研究。有NSHL家族史的先证者家族中至少有两名听力受损受试者。零星的
METHODS Subjects Independently ascertained probands (n= 215) were recruited for the study. Probands with a family history of NSHL had at least two hearing impaired subjects in the family. Sporadic