Complete Exon–Intron Structure of the Retina-Specific ATP Binding Transporter Gene (ABCR) Allows the Identification of Novel Mutations Underlying Stargardt Disease-Reference-Cited by-同舟云学术

Complete Exon–Intron Structure of the Retina-Specific ATP Binding Transporter Gene (ABCR) Allows the Identification of Novel Mutations Underlying Stargardt Disease

Published:1998-02 Issue:1 Volume:48 Page:139-142
ISSN:0888-7543
Container-title:Genomics
language:en
Short-container-title:Genomics

Author:

Gerber S.,Rozet J.M.,van de Pol T.J.R.,Hoyng C.B.,Munnich A.,Blankenagel A.,Kaplan J.,Cremers F.P.M.

Publisher

Elsevier BV

Subject

Genetics

Reference9 articles.

1. A photoreceptor cell-specific ATP-binding transporter gene (ABCR;Allikmets;Nat. Genet.,1997

2. Correction. A photoreceptor cell-specific ATP-binding transporter gene (ABCR;Allikmets;Nat. Genet.,1997

3. Mutation of the Stargardt disease gene (ABCR;Allikmets;Science,1997

4. A gene for late-onset fundus flavimaculatus with macular dystrophy maps to chromosome 1p13;Gerber;Am. J. Hum. Genet.,1995

5. A gene for Stargardt's disease (fundus flavimaculatus;Gerber;Nat. Genet.,1993

Cited by 64 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Spectrum of variants associated with inherited retinal dystrophies in Northeast Mexico;BMC Ophthalmology;2024-02-12

2. Genotype–Phenotype Association in ABCA4-Associated Retinopathy;Retinal Degenerative Diseases XIX;2023

3. Clinical and Genetic Correlations of Inherital Retinal Disease with Mutations in the ABCA4 Gene by Patients of the Russian Population;Ophthalmology in Russia;2021-12-29

4. Structure and function of ABCA4 and its role in the visual cycle and Stargardt macular degeneration;Progress in Retinal and Eye Research;2021-12

5. Whole genome sequencing and in vitro splice assays reveal genetic causes for inherited retinal diseases;npj Genomic Medicine;2021-11-18