Human RTEL1 deficiency causes Hoyeraal–Hreidarsson syndrome with short telomeres and genome instability
出版年份 2013 全文链接
标题
Human RTEL1 deficiency causes Hoyeraal–Hreidarsson syndrome with short telomeres and genome instability
作者
关键词
-
出版物
HUMAN MOLECULAR GENETICS
Volume 22, Issue 16, Pages 3239-3249
出版商
Oxford University Press (OUP)
发表日期
2013-04-17
DOI
10.1093/hmg/ddt178
参考文献
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注意:仅列出部分参考文献,下载原文获取全部文献信息。- Germline mutations of regulator of telomere elongation helicase 1, RTEL1, in Dyskeratosis congenita
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