PRPH2 mutation as the cause of various clinical manifestations in a family affected with inherited retinal dystrophy

标题
PRPH2 mutation as the cause of various clinical manifestations in a family affected with inherited retinal dystrophy
作者
关键词
-
出版物
OPHTHALMIC GENETICS
Volume 40, Issue 5, Pages 436-442
出版商
Informa UK Limited
发表日期
2019-10-17
DOI
10.1080/13816810.2019.1678178

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