A novel mutation in retinitis pigmentosa GTPase regulator gene with a distinctive retinitis pigmentosa phenotype in a Chinese family.
about
Reappearance of the tapetal-like reflex after prolonged dark adaptation in a female carrier of RPGR ORF15 X-linked retinitis pigmentosa.Genetic analysis of Chinese families reveals a novel truncation allele of the retinitis pigmentosa GTPase regulator gene.Identification of novel CYP4V2 gene mutations in 92 Chinese families with Bietti's crystalline corneoretinal dystrophy.Good epidemiologic practice in retinitis pigmentosa: from phenotyping to biobanking.Identification of novel X-linked gain-of-function RPGR-ORF15 mutation in Italian family with retinitis pigmentosa and pathologic myopia
P2860
A novel mutation in retinitis pigmentosa GTPase regulator gene with a distinctive retinitis pigmentosa phenotype in a Chinese family.
description
2010 nî lūn-bûn
@nan
2010 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
A novel mutation in retinitis ...... phenotype in a Chinese family.
@ast
A novel mutation in retinitis ...... phenotype in a Chinese family.
@en
A novel mutation in retinitis ...... phenotype in a Chinese family.
@nl
type
label
A novel mutation in retinitis ...... phenotype in a Chinese family.
@ast
A novel mutation in retinitis ...... phenotype in a Chinese family.
@en
A novel mutation in retinitis ...... phenotype in a Chinese family.
@nl
prefLabel
A novel mutation in retinitis ...... phenotype in a Chinese family.
@ast
A novel mutation in retinitis ...... phenotype in a Chinese family.
@en
A novel mutation in retinitis ...... phenotype in a Chinese family.
@nl
P2093
P2860
P1433
P1476
A novel mutation in retinitis ...... phenotype in a Chinese family
@en
P2093
Hongwang Ren
Ruihua Meng
Weining Rong
Wenjuan Zhuang
Xinfang Zhang
Xunlun Sheng
P2860
P304
P577
2010-08-15T00:00:00Z