Identification of a novel RPGRIP1 mutation in an Iranian family with leber congenital amaurosis by exome sequencing.
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Identification of a novel RPGRIP1 mutation in an Iranian family with leber congenital amaurosis by exome sequencing.
description
2017 nî lūn-bûn
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2017年の論文
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2017年学术文章
@wuu
2017年学术文章
@zh
2017年学术文章
@zh-cn
2017年学术文章
@zh-hans
2017年学术文章
@zh-my
2017年学术文章
@zh-sg
2017年學術文章
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2017年學術文章
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name
Identification of a novel RPGR ...... amaurosis by exome sequencing.
@en
Identification of a novel RPGR ...... amaurosis by exome sequencing.
@nl
type
label
Identification of a novel RPGR ...... amaurosis by exome sequencing.
@en
Identification of a novel RPGR ...... amaurosis by exome sequencing.
@nl
prefLabel
Identification of a novel RPGR ...... amaurosis by exome sequencing.
@en
Identification of a novel RPGR ...... amaurosis by exome sequencing.
@nl
P2093
P2860
P356
P1476
Identification of a novel RPGR ...... amaurosis by exome sequencing.
@en
P2093
Abdolkarim Mobasher-Jannat
Chunli Wei
Jingliang Cheng
Khosrow Jadidi
Lisha Yang
Marzieh Dehghan Shasaltaneh
Saber Imani
Saman Mohazzab-Torabi
Shangyi Fu
P2860
P304
P356
10.1111/JCMM.13454
P577
2017-11-29T00:00:00Z