Clinical and Molecular Characteristics of Childhood-Onset Stargardt Disease-Reference-Cited by-同舟云学术

Clinical and Molecular Characteristics of Childhood-Onset Stargardt Disease

Published:2015-02 Issue:2 Volume:122 Page:326-334
ISSN:0161-6420
Container-title:Ophthalmology
language:en
Short-container-title:Ophthalmology

Author:

Fujinami Kaoru,Zernant Jana,Chana Ravinder K.,Wright Genevieve A.,Tsunoda Kazushige,Ozawa Yoko^ORCID,Tsubota Kazuo,Robson Anthony G.,Holder Graham E.,Allikmets Rando,Michaelides Michel,Moore Anthony T.

Publisher

Elsevier BV

Subject

Ophthalmology

Reference41 articles.

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

3. Fundus flavimaculatus. A clinical classification;Fishman;Arch Ophthalmol,1976

4. ABCA4 mutations and discordant ABCA4 alleles in patients and siblings with bull's-eye maculopathy;Michaelides;Br J Ophthalmol,2007

5. A longitudinal study of Stargardt disease: clinical and electrophysiologic assessment, progression, and genotype correlations;Fujinami;Am J Ophthalmol,2013

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