Recessive and dominant mutations in COL12A1 cause a novel EDS/myopathy overlap syndrome in humans and mice

标题
Recessive and dominant mutations in COL12A1 cause a novel EDS/myopathy overlap syndrome in humans and mice
作者
关键词
-
出版物
HUMAN MOLECULAR GENETICS
Volume 23, Issue 9, Pages 2339-2352
出版商
Oxford University Press (OUP)
发表日期
2013-12-12
DOI
10.1093/hmg/ddt627

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