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	Co-Existence of Novel PDE6A Mutations and A Recurrent RPGR Mutation: A Potential Explanation for Phenotypic Diversity in Female RPGR Mutation Carriers
	Chen, X.; Sheng, X.; Liu, G.; Liu, Y.; Li, H.; Xie, P.; Liu, Q.; Yan, B.; Zhao, C.
刊名	CURRENT MOLECULAR MEDICINE
	2018
卷号	18期号:5
关键词	Retinitis pigmentosa X-linked mutation RPGR PDE6A genotype-phenotype correlation
ISSN号	1566-5240
URL标识	查看原文
语种	英语
内容类型	期刊论文
URI标识	http://www.corc.org.cn/handle/1471x/3608692
专题	复旦大学上海医学院
推荐引用方式 GB/T 7714	Chen, X.,Sheng, X.,Liu, G.,et al. Co-Existence of Novel PDE6A Mutations and A Recurrent RPGR Mutation: A Potential Explanation for Phenotypic Diversity in Female RPGR Mutation Carriers[J]. CURRENT MOLECULAR MEDICINE,2018,18(5).
APA	Chen, X..,Sheng, X..,Liu, G..,Liu, Y..,Li, H..,...&Zhao, C..(2018).Co-Existence of Novel PDE6A Mutations and A Recurrent RPGR Mutation: A Potential Explanation for Phenotypic Diversity in Female RPGR Mutation Carriers.CURRENT MOLECULAR MEDICINE,18(5).
MLA	Chen, X.,et al."Co-Existence of Novel PDE6A Mutations and A Recurrent RPGR Mutation: A Potential Explanation for Phenotypic Diversity in Female RPGR Mutation Carriers".CURRENT MOLECULAR MEDICINE 18.5(2018).

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