A gene (RPGR) with homology to the RCC1 guanine nucleotide exchange factor is mutated in X–linked retinitis pigmentosa (RP3)-Reference-Cited by-同舟云学术

A gene (RPGR) with homology to the RCC1 guanine nucleotide exchange factor is mutated in X–linked retinitis pigmentosa (RP3)

Published:1996-05 Issue:1 Volume:13 Page:35-42
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Meindl A.,Dry K.,Herrmann K.,Manson E.,Ciccodicola A.,Edgar A.,Carvalho M.R.S.,Achatz H.,Hellebrand H.,Lennon A.,Migliaccio C.,Porter K.,Zrenner E.,Bird A.,Jay M.,Lorenz B.,Wittwer B.,D'Urso M.,Meitinger T.,Wright A.

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng0596-35.pdf

Reference53 articles.

1. Heckenlively, J.R. Retinitis Pigmentosa 1–269 (Lippincott Company, Philadelphia, 1988).

2. Dryja, T.P. & Li, T. Molecular genetics of retinitis pigmentosa. Hum. Molec. Genet. 4, 1739–1743 (1995).

3. Bircl, A.C. X-linked retinitis pigmentosa. Br. J. Ophthalmol. 59, 177–199 (1975).

4. Fishman, G.A., Farber, M.D. & Deriacki, D.J. X-linked retinitis pigmentosa: profile of clinical findings. Arch. Ophthalmol. 106, 369–375 (1988).

5. Jay, M. On the heredity of retinitis pigmentosa. Br. J. Ophthalmol. 66, 405–416 (1982).

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