Biallelic Mutation of ARHGEF18, Involved in the Determination of Epithelial Apicobasal Polarity, Causes Adult-Onset Retinal Degeneration.
about
Mapping the genomic landscape of inherited retinal disease genes prioritizes genes prone to coding and noncoding copy-number variations.A new perspective on the genetics of keratoconus: why have we not been more successful?Expression of novel "LOCGEF" isoforms of ARHGEF18 in eosinophils.Association between a Single Nucleotide Polymorphism in the 3'-UTR of and the Risk of Nonidiopathic Pulmonary Arterial Hypertension in Chinese Population
P2860
Biallelic Mutation of ARHGEF18, Involved in the Determination of Epithelial Apicobasal Polarity, Causes Adult-Onset Retinal Degeneration.
description
2017 nî lūn-bûn
@nan
2017年の論文
@ja
2017年論文
@yue
2017年論文
@zh-hant
2017年論文
@zh-hk
2017年論文
@zh-mo
2017年論文
@zh-tw
2017年论文
@wuu
2017年论文
@zh
2017年论文
@zh-cn
name
Biallelic Mutation of ARHGEF18 ...... lt-Onset Retinal Degeneration.
@en
Biallelic Mutation of ARHGEF18 ...... lt-Onset Retinal Degeneration.
@nl
type
label
Biallelic Mutation of ARHGEF18 ...... lt-Onset Retinal Degeneration.
@en
Biallelic Mutation of ARHGEF18 ...... lt-Onset Retinal Degeneration.
@nl
prefLabel
Biallelic Mutation of ARHGEF18 ...... lt-Onset Retinal Degeneration.
@en
Biallelic Mutation of ARHGEF18 ...... lt-Onset Retinal Degeneration.
@nl
P2093
P2860
P50
P1476
Biallelic Mutation of ARHGEF18 ...... lt-Onset Retinal Degeneration.
@en
P2093
Alessia Fiorentino
Andrew R Webster
Anthony G Robson
Anthony T Moore
Ceniz Zihni
F Lucy Raymond
Gavin Arno
Graham E Holder
Karl Matter
NIHR Bioresource - Rare Diseases Consortium
P2860
P304
P356
10.1016/J.AJHG.2016.12.014
P407
P577
2017-01-21T00:00:00Z