Whole-Exome Sequencing Identifies Mutations of KIF22 in Spondyloepimetaphyseal Dysplasia with Joint Laxity, Leptodactylic Type

标题
Whole-Exome Sequencing Identifies Mutations of KIF22 in Spondyloepimetaphyseal Dysplasia with Joint Laxity, Leptodactylic Type
作者
关键词
-
出版物
AMERICAN JOURNAL OF HUMAN GENETICS
Volume 89, Issue 6, Pages 760-766
出版商
Elsevier BV
发表日期
2011-12-11
DOI
10.1016/j.ajhg.2011.10.015

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