Mutations in CEP78 Cause Cone-Rod Dystrophy and Hearing Loss Associated with Primary-Cilia Defects

标题
Mutations in CEP78 Cause Cone-Rod Dystrophy and Hearing Loss Associated with Primary-Cilia Defects
作者
关键词
-
出版物
AMERICAN JOURNAL OF HUMAN GENETICS
Volume 99, Issue 3, Pages 770-776
出版商
Elsevier BV
发表日期
2016-09-03
DOI
10.1016/j.ajhg.2016.07.009

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