Mutations in the ABCA4 (ABCR) Gene Are the Major Cause of Autosomal Recessive Cone-Rod Dystrophy-Reference-Cited by-同舟云学术

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Mutations in the ABCA4 (ABCR) Gene Are the Major Cause of Autosomal Recessive Cone-Rod Dystrophy

Published:2000-10 Issue:4 Volume:67 Page:960-966
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Maugeri Alessandra,Klevering B. Jeroen,Rohrschneider Klaus,Blankenagel Anita,Brunner Han G.,Deutman August F.,Hoyng Carel B.,Cremers Frans P.M.

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference30 articles.

1. Molecular genetics of age-related macular degeneration: current status;Allikmets;Eur J Ophthalmol,1999

2. Further evidence for an association of ABCR alleles with age-related macular degeneration;Allikmets;Am J Hum Genet,2000

3. Mutation of the Stargardt disease gene (ABCR) in age-related macular degeneration;Allikmets;Science,1997

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

5. Apoptosis: final common pathway of photoreceptor death in rd, rds, and rhodopsin mutant mice;Chang;Neuron,1993

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