(Q43903067)

27 November 2017

title

A distinctive form of congenital stationary night blindness with cone ON-pathway dysfunction (English)

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congenital stationary night blindness

27 November 2017

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author name string

Claire S Barnes

series ordinal

1

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27 November 2017

Kenneth R Alexander

series ordinal

2

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27 November 2017

Gerald A Fishman

series ordinal

3

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27 November 2017

publication date

1 March 2002

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27 November 2017

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27 November 2017

volume

109

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27 November 2017

issue

3

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27 November 2017

page(s)

575-583

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[Analysis of the human electroretinogram]

27 November 2017

cites work

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Autosomal dominant congenital stationary night blindness and normal fundus with an electronegative electroretinogram

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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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A Japanese pedigree of autosomal dominant congenital stationary night blindness with variable expressivity

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Congenital stationary night blindness presenting as Leber's congenital amaurosis

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X-linked congenital stationary night blindness. Review and report of a family with hyperopia

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

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Congenital stationary night blindness with negative electroretinogram. A new classification

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Increased phase lag of the fundamental harmonic component of the 30 Hz flicker ERG in Schubert-Bornschein complete type CSNB

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7 January 2021

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

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Loss-of-function mutations in a calcium-channel alpha1-subunit gene in Xp11.23 cause incomplete X-linked congenital stationary night blindness

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

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Gene for autosomal dominant congenital stationary night blindness maps to the same region as the gene for the beta-subunit of the rod photoreceptor cGMP phosphodiesterase (PDEB) in chromosome 4p16.3.

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Temporal frequency deficits in the electroretinogram of the cone system in X-linked retinoschisis

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7 January 2021

ON-pathway dysfunction in a patient with acquired unilateral night blindness

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7 January 2021

2-Amino-4-Phosphonobutyric Acid: A New Pharmacological Tool for Retina Research

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7 January 2021

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7 January 2021

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Identifiers

DOI

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27 November 2017

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