Mutations in SEC24D, Encoding a Component of the COPII Machinery, Cause a Syndromic Form of Osteogenesis Imperfecta

标题
Mutations in SEC24D, Encoding a Component of the COPII Machinery, Cause a Syndromic Form of Osteogenesis Imperfecta
作者
关键词
-
出版物
AMERICAN JOURNAL OF HUMAN GENETICS
Volume 96, Issue 3, Pages 432-439
出版商
Elsevier BV
发表日期
2015-02-13
DOI
10.1016/j.ajhg.2015.01.002

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