Phenotype of retinitis pigmentosa associated with the Ser50Thr mutation in the NRL gene
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Recessive NRL mutations in patients with clumped pigmentary retinal degeneration and relative preservation of blue cone functionRecurrent mutation in the first zinc finger of the orphan nuclear receptor NR2E3 causes autosomal dominant retinitis pigmentosaNovel p.M96T variant of NRL and shRNA-based suppression and replacement of NRL mutants associated with autosomal dominant retinitis pigmentosa.Early visual symptom patterns in inherited retinal dystrophies.Autosomal Recessive NRL Mutations in Patients with Enhanced S-Cone Syndrome.
P2860
Phenotype of retinitis pigmentosa associated with the Ser50Thr mutation in the NRL gene
description
2003 nî lūn-bûn
@nan
2003 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2003 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2003年の論文
@ja
2003年論文
@yue
2003年論文
@zh-hant
2003年論文
@zh-hk
2003年論文
@zh-mo
2003年論文
@zh-tw
2003年论文
@wuu
name
Phenotype of retinitis pigmentosa associated with the Ser50Thr mutation in the NRL gene
@ast
Phenotype of retinitis pigmentosa associated with the Ser50Thr mutation in the NRL gene
@en
Phenotype of retinitis pigmentosa associated with the Ser50Thr mutation in the NRL gene
@nl
type
label
Phenotype of retinitis pigmentosa associated with the Ser50Thr mutation in the NRL gene
@ast
Phenotype of retinitis pigmentosa associated with the Ser50Thr mutation in the NRL gene
@en
Phenotype of retinitis pigmentosa associated with the Ser50Thr mutation in the NRL gene
@nl
prefLabel
Phenotype of retinitis pigmentosa associated with the Ser50Thr mutation in the NRL gene
@ast
Phenotype of retinitis pigmentosa associated with the Ser50Thr mutation in the NRL gene
@en
Phenotype of retinitis pigmentosa associated with the Ser50Thr mutation in the NRL gene
@nl
P2093
P1433
P1476
Phenotype of retinitis pigmentosa associated with the Ser50Thr mutation in the NRL gene
@en
P2093
Alan C Bird
David A R Bessant
Frederick W Fitzke
Graham E Holder
Shomi S Bhattacharya
P304
P356
10.1001/ARCHOPHT.121.6.793
P407
P577
2003-06-01T00:00:00Z