Outer retinal structural anomaly due to frameshift mutation in CACNA1F gene.

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Amyloid Precursor-Like Protein 2 deletion-induced retinal synaptopathy related to congenital stationary night blindness: structural, functional and molecular characteristics Channeling Vision: CaV1.4-A Critical Link in Retinal Signal Transmission.

P2860

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P2860

Outer retinal structural anomaly due to frameshift mutation in CACNA1F gene.

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http://www.wikidata.org/entity/Q42325649

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2012 nî lūn-bûn

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2012年の論文

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2012年論文

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2012年論文

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2012年論文

@zh-hk

2012年論文

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@zh-tw

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Outer retinal structural anomaly due to frameshift mutation in CACNA1F gene.

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Outer retinal structural anomaly due to frameshift mutation in CACNA1F gene.

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Outer retinal structural anomaly due to frameshift mutation in CACNA1F gene.

@en

Outer retinal structural anomaly due to frameshift mutation in CACNA1F gene.

@nl

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Outer retinal structural anomaly due to frameshift mutation in CACNA1F gene.

@en

Outer retinal structural anomaly due to frameshift mutation in CACNA1F gene.

@nl

P1476

Outer retinal structural anomaly due to frameshift mutation in CACNA1F gene

@en

P2093

E Héon

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P2860

Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness

An L-type calcium-channel gene mutated in incomplete X-linked congenital stationary night blindness

Mutation of the calcium channel gene Cacna1f disrupts calcium signaling, synaptic transmission and cellular organization in mouse retina

The nob2 mouse, a null mutation in Cacna1f: anatomical and functional abnormalities in the outer retina and their consequences on ganglion cell visual responses

Human photoreceptor topography.

Autofluorescence imaging and spectral-domain optical coherence tomography in incomplete congenital stationary night blindness and comparison with retinitis pigmentosa

A novel p.Gly603Arg mutation in CACNA1F causes Åland island eye disease and incomplete congenital stationary night blindness phenotypes in a family.

Immunohistochemical analysis of the outer plexiform layer in the nob mouse shows no abnormalities.

Early afferent signaling in the outer plexiform layer regulates development of horizontal cell morphology.

P2888

eye.2012.125

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1278-1280

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scholarly article

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10.1038/EYE.2012.125

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Ajoy Vincent

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2012-06-29T00:00:00Z

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Outer retinal structural anomaly due to frameshift mutation in CACNA1F gene.

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P2860

P2860

Outer retinal structural anomaly due to frameshift mutation in CACNA1F gene.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P433

P478

P50

P577

P6179

P698

P932

P356

P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P433

P478

P50

P577

P6179

P698

P932