Visual Function in Patients with Cone–Rod Dystrophy (CRD) Associated with Mutations in theABCA4 (ABCR) Gene-Reference-Cited by-同舟云学术

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Visual Function in Patients with Cone–Rod Dystrophy (CRD) Associated with Mutations in theABCA4 (ABCR) Gene

Published:2001-12 Issue:6 Volume:73 Page:877-886
ISSN:0014-4835
Container-title:Experimental Eye Research
language:en
Short-container-title:Experimental Eye Research

Author:

Birch David G.,Peters Angela Y.,Locke Kirsten L.,Spencer Rand,Megarity Christine F.,Travis Gabriel H.

Publisher

Elsevier BV

Subject

Cellular and Molecular Neuroscience,Sensory Systems,Ophthalmology

Reference42 articles.

1. The effect of lipid environment and retinoids on the ATPase activity of ABCR, the photoreceptor transporter responsible for Stargardt macular dystrophy;Ahn;J. Biol. Chem.,2000

2. A photoreceptor cell-specific ATP-binding transporter gene (ABCR) is mutated in recessive Stargardt macular dystrophy;Allikmets;Nat. Genet.,1997

3. Fundus fluorescein angiography in fundus flavimaculatus and Stargardts disease;Anmarkrud;Acta Ophthalmol.,1979

4. The photoreceptor rim protein is an ABC transporter encoded by the gene for recessive Stargardt's disease (ABCR);Azarian;FEBS Lett.,1997

5. Progressive cone–rod degeneration;Berson;Arch. Ophthalmol.,1968

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