Whole-exome sequencing identifies rare, functional CFH variants in families with macular degeneration
出版年份 2014 全文链接
标题
Whole-exome sequencing identifies rare, functional CFH variants in families with macular degeneration
作者
关键词
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出版物
HUMAN MOLECULAR GENETICS
Volume 23, Issue 19, Pages 5283-5293
出版商
Oxford University Press (OUP)
发表日期
2014-05-21
DOI
10.1093/hmg/ddu226
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