Retinal–specific guanylate cyclase gene mutations in Leber's congenital amaurosis-Reference-Cited by-同舟云学术

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

Published:1996-12 Issue:4 Volume:14 Page:461-464
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Perrault Isabella,Rozet Jean Michel,Calvas Patrick,Gerber Sylvie,Camuzat Agnès,Dollfus Hélène,Châtelin Sophie,Souied Eric,Ghazi Ihmad,Leowski Corinne,Bonnemaison Michel,Paslier Denis Le,Frézal Jean,Dufier Jean-Louis,Pittler Steven,Munnich Arnold,Kaplan Josseline

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng1296-461.pdf

Reference30 articles.

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2. Foxman, S.G., Heckenlively, J.R., Batemen, B.J. & Wirstschafter, J.D. Classification of congenital and early-onset retinitis pigmentosa. Arch. Ophthalmol. 103, 1502–1507 (1985).

3. Kaplan, J., Bonneau, D., Frézal, J., Munnich, A. & Dufier, J.L. Clinical and genetic heterogeneity in retinitis pigmentosa. Hum. Genet. 85, 635–642 (1990).

4. Franceschetti, A. & Dieterle, P. L'importance diagnostique de l'électrorétinogramme dans les dégénérescences tapéto-rétiniennes avec rétrécissement du champ visuel et héméralopie. Conf. Neurol. 14, 184–186 (1954).

5. Franceschetti, A & Forni, S. Dégénérescence tapéto-rétinienne (type Leber) avec aspect marbré du fond de I'oeil périphérique. Ophthalmologies 135, 610–616 (1958).

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