Mutations in the human retinal degeneration slow (RDS) gene can cause either retinitis pigmentosa or macular dystrophy-Reference-Cited by-同舟云学术

Mutations in the human retinal degeneration slow (RDS) gene can cause either retinitis pigmentosa or macular dystrophy

Published:1993-03 Issue:3 Volume:3 Page:213-218
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Wells John,Wroblewski John,Keen Jeffrey,Inglehearn Christopher,Jubb Christopher,Eckstein Anja,Jay Marcelle,Arden Geoffrey,Bhattacharya Shomi,Fitzke Fred,Bird Alan

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng0393-213.pdf

Reference26 articles.

1. McWilliam, P. et al. Autosomal dominant retinitis pigmentosa (ADRP): Localization of an ADRP gene to the long arm of chromosome 3. Genomics 5, 619–622 (1989).

2. Dryja, T.P. et al. A point mutation of the rhodopsin gene in one form of retinitis pigmentosa. Nature 343, 364–366 (1990).

3. Dryja, T.P. et al. Mutations within the rhodopsin gene in patients with autosomal dominant retinitis pigmentosa. New Engl. J. Med. 323, 1302–1307 (1990).

4. Sung, C.H. et al. Rhodopsin mutations in autosomal dominant retinitis pigmentosa. Proc. natn. Acad. Sci. U.S.A. 88, 6481–6485 (1991).

5. Keen, T.J. et al. Autosomal dominant retinitis pigmentosa: four new mutations in rhodopsin, one of them at the retinal attachment site. Genomics, 11, 199–205 (1991).

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