Assessment of night vision problems in patients with congenital stationary night blindness - Wikidata - awgldk - TriplyDB

Assessment of night vision problems in patients with congenital stationary night blindness

Assessment of night vision problems in patients with congenital stationary night blindness

http://www.wikidata.org/entity/Q34712842

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Voltage-Gated Cav1 Channels in Disorders of Vision and Hearing Neurobiological hypothesis of color appearance and hue perception Voriconazole, an antifungal triazol that causes visual side effects, is an inhibitor of TRPM1 and TRPM3 channels Presentation of TRPM1-Associated Congenital Stationary Night Blindness in Children.Channeling Vision: CaV1.4-A Critical Link in Retinal Signal Transmission.

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Assessment of night vision problems in patients with congenital stationary night blindness

http://www.wikidata.org/entity/Q34712842

description

2013 nî lūn-bûn

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2013 թուականի Մայիսին հրատարակուած գիտական յօդուած

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2013 թվականի մայիսին հրատարակված գիտական հոդված

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2013年の論文

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2013年論文

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2013年論文

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2013年論文

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2013年論文

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2013年論文

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2013年论文

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name

Assessment of night vision pro ...... tal stationary night blindness

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Assessment of night vision pro ...... tal stationary night blindness

@en

Assessment of night vision pro ...... tal stationary night blindness

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type

label

Assessment of night vision pro ...... tal stationary night blindness

@ast

Assessment of night vision pro ...... tal stationary night blindness

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Assessment of night vision pro ...... tal stationary night blindness

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Assessment of night vision pro ...... tal stationary night blindness

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Assessment of night vision pro ...... tal stationary night blindness

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Assessment of night vision pro ...... tal stationary night blindness

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Assessment of night vision pro ...... tal stationary night blindness

@en

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Amir A Katzin

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Astrid M L Kappers

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Frank P Hoeben

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Frans C C Riemslag

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Maria M van Genderen

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Mieke M C Bijveld

http://www.w3.org/2001/XMLSchema#string

Ruth M A van Nispen

http://www.w3.org/2001/XMLSchema#string

P2860

Whole-exome sequencing identifies mutations in GPR179 leading to autosomal-recessive complete congenital stationary night blindness

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

Mutations in CABP4, the gene encoding the Ca2+-binding protein 4, cause autosomal recessive night blindness

The electroretinographic diagnosis of the incomplete form of congenital stationary night blindness

Recessive mutations of the gene TRPM1 abrogate ON bipolar cell function and cause complete congenital stationary night blindness in humans

Mutations in TRPM1 are a common cause of complete congenital stationary night blindness

Night blindness and abnormal cone electroretinogram ON responses in patients with mutations in the GRM6 gene encoding mGluR6

Genotype-phenotype correlation in British families with X linked congenital stationary night blindness

Clinical variability among patients with incomplete X-linked congenital stationary night blindness and a founder mutation in CACNA1F

The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat protein

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e62927

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scholarly article

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10.1371/JOURNAL.PONE.0062927

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236666823

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23658786

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congenital stationary night blindness

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3643903

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