Recovery of Visual Functions in a Mouse Model of Leber Congenital Amaurosis-Reference-Cited by-同舟云学术

Recovery of Visual Functions in a Mouse Model of Leber Congenital Amaurosis

Published:2002-05 Issue:21 Volume:277 Page:19173-19182
ISSN:0021-9258
Container-title:Journal of Biological Chemistry
language:en
Short-container-title:Journal of Biological Chemistry

Author:

Van Hooser J. Preston,Liang Yan,Maeda Tadao,Kuksa Vladimir,Jang Geeng-Fu,He Yu-Guang,Rieke Fred,Fong Henry K.W.,Detwiler Peter B.,Palczewski Krzysztof

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry

Reference39 articles.

1. Mutations in RPE65 cause autosomal recessive childhood–onset severe retinal dystrophy

2. Retinal–specific guanylate cyclase gene mutations in Leber's congenital amaurosis

3. Leber congenital amaurosis caused by a homozygous mutation (R90W) in the homeodomain of the retinal transcription factor CRX: direct evidence for the involvement of CRX in the development of photoreceptor function

4. Mutations in a new photoreceptor-pineal gene on 17p cause Leber congenital amaurosis

5. Complete exon-intron structure of the RPGR-interacting protein (RPGRIP1) gene allows the identification of mutations underlying Leber congenital amaurosis

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