A novel loss-of-function mutation in Npr2 clarifies primary role in female reproduction and reveals a potential therapy for acromesomelic dysplasia, Maroteaux type
出版年份 2012 全文链接
标题
A novel loss-of-function mutation in Npr2 clarifies primary role in female reproduction and reveals a potential therapy for acromesomelic dysplasia, Maroteaux type
作者
关键词
-
出版物
HUMAN MOLECULAR GENETICS
Volume 22, Issue 2, Pages 345-357
出版商
Oxford University Press (OUP)
发表日期
2012-10-14
DOI
10.1093/hmg/dds432
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