Mutation ofIFNLR1, an interferon lambda receptor 1, is associated with autosomal-dominant non-syndromic hearing loss
出版年份 2018 全文链接
标题
Mutation ofIFNLR1, an interferon lambda receptor 1, is associated with autosomal-dominant non-syndromic hearing loss
作者
关键词
-
出版物
JOURNAL OF MEDICAL GENETICS
Volume 55, Issue 5, Pages 298-306
出版商
BMJ
发表日期
2018-02-17
DOI
10.1136/jmedgenet-2017-104954
参考文献
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