Cosegregation and functional analysis of mutant ABCR (ABCA4) alleles in families that manifest both Stargardt disease and age-related macular degeneration-Reference-Cited by-同舟云学术

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Cosegregation and functional analysis of mutant ABCR (ABCA4) alleles in families that manifest both Stargardt disease and age-related macular degeneration

Published:2001-11-01 Issue:23 Volume:10 Page:2671-2678
ISSN:1460-2083
Container-title:Human Molecular Genetics
language:
Short-container-title:

Author:

Shroyer N. F.

Publisher

Oxford University Press (OUP)

Subject

Genetics(clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/10/23/2671/9813572/102671.pdf

Cited by 108 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

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2. Retinoic acid related orphan receptor α is a genetic modifier that rescues retinal degeneration in a mouse model of Stargardt disease and Dry AMD;Gene Therapy;2024-05-16

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

4. Functional characterization of ABCA4 genetic variants related to Stargardt disease;Scientific Reports;2022-12-24

5. Effective splicing restoration of a deep-intronic ABCA4 variant in cone photoreceptor precursor cells by CRISPR/SpCas9 approaches;Molecular Therapy - Nucleic Acids;2022-09

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