A Point Mutation in PDGFRB Causes Autosomal-Dominant Penttinen Syndrome

标题
A Point Mutation in PDGFRB Causes Autosomal-Dominant Penttinen Syndrome
作者
关键词
-
出版物
AMERICAN JOURNAL OF HUMAN GENETICS
Volume 97, Issue 3, Pages 465-474
出版商
Elsevier BV
发表日期
2015-08-14
DOI
10.1016/j.ajhg.2015.07.009

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