Clinical Phenotypes and Prognostic Full-Field Electroretinographic Findings in Stargardt Disease-Reference-Cited by-同舟云学术

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Clinical Phenotypes and Prognostic Full-Field Electroretinographic Findings in Stargardt Disease

Published:2013-03 Issue:3 Volume:155 Page:465-473.e3
ISSN:0002-9394
Container-title:American Journal of Ophthalmology
language:en
Short-container-title:American Journal of Ophthalmology

Author:

Zahid Sarwar,Jayasundera Thiran,Rhoades William,Branham Kari,Khan Naheed,Niziol Leslie M.,Musch David C.,Heckenlively John R.

Funder

Foundation Fighting Blindness

National Eye Institute

Research to Prevent Blindness

Publisher

Elsevier BV

Subject

Ophthalmology

Reference30 articles.

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

2. Retinitis pigmentosa in Spain. The Spanish Multicentric and Multidisciplinary Group for Research into Retinitis Pigmentosa;Ayuso;Clin Genet,1995

3. Fundus flavimaculatus;Blacharski,1988

4. A new locus for autosomal recessive retinitis pigmentosa (RP19) maps to 1p13–1p21;Martinez-Mir;Genomics,1997

5. Retinitis pigmentosa caused by a homozygous mutation in the Stargardt disease gene ABCR;Martinez-Mir;Nat Genet,1998

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