Usher syndromes due to MYO7A, PCDH15, USH2A or GPR98 mutations share retinal disease mechanism

标题
Usher syndromes due to MYO7A, PCDH15, USH2A or GPR98 mutations share retinal disease mechanism
作者
关键词
-
出版物
HUMAN MOLECULAR GENETICS
Volume 17, Issue 15, Pages 2405-2415
出版商
Oxford University Press (OUP)
发表日期
2008-05-08
DOI
10.1093/hmg/ddn140

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