Slow and fast rod ERG pathways in patients with X-linked complete stationary night blindness carrying mutations in the NYX gene.
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Mutations in TRPM1 are a common cause of complete congenital stationary night blindnessNight blindness and abnormal cone electroretinogram ON responses in patients with mutations in the GRM6 gene encoding mGluR6Genotype-phenotype correlation in British families with X linked congenital stationary night blindnessRod-driven OFF pathway responses in the distal retina: dark-adapted flicker electroretinogram in mouseGenetic variations strongly influence phenotypic outcome in the mouse retina.TRPM1 mutations are associated with the complete form of congenital stationary night blindnessA novel p.Gly603Arg mutation in CACNA1F causes Åland island eye disease and incomplete congenital stationary night blindness phenotypes in a family.The special electrophysiological signs of inherited retinal dystrophiesPhotoreceptor and postreceptor responses in congenital stationary night blindness.Ultrastructural localization of GPR179 and the impact of mutant forms on retinal function in CSNB1 patients and a mouse model.
P2860
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P2860
Slow and fast rod ERG pathways in patients with X-linked complete stationary night blindness carrying mutations in the NYX gene.
description
2001 nî lūn-bûn
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2001年の論文
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2001年学术文章
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2001年学术文章
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name
Slow and fast rod ERG pathways ...... ing mutations in the NYX gene.
@en
Slow and fast rod ERG pathways ...... ing mutations in the NYX gene.
@nl
type
label
Slow and fast rod ERG pathways ...... ing mutations in the NYX gene.
@en
Slow and fast rod ERG pathways ...... ing mutations in the NYX gene.
@nl
prefLabel
Slow and fast rod ERG pathways ...... ing mutations in the NYX gene.
@en
Slow and fast rod ERG pathways ...... ing mutations in the NYX gene.
@nl
P2093
P1476
Slow and fast rod ERG pathways ...... ing mutations in the NYX gene.
@en
P2093
Apfelstedt-Sylla E
Langrová H
Wissinger B
P304
P407
P577
2001-10-01T00:00:00Z