Clinical Features of Autosomal Dominant Retinitis Pigmentosa With Rhodopsin Gene Codon 17 Mutation and Retinal Neovascularization in a Japanese Patient-Reference-Cited by-同舟云学术

Clinical Features of Autosomal Dominant Retinitis Pigmentosa With Rhodopsin Gene Codon 17 Mutation and Retinal Neovascularization in a Japanese Patient

Published:1993-02 Issue:2 Volume:115 Page:168-173
ISSN:0002-9394
Container-title:American Journal of Ophthalmology
language:en
Short-container-title:American Journal of Ophthalmology

Author:

Hayakawa Mutsuko,Hotta Yoshihiro,Imai Yoshie,Fujiki Keiko,Nakamura Atsuo,Yanashima Kenji,Kanai Atsushi

Publisher

Elsevier BV

Subject

Ophthalmology

Reference29 articles.

1. A point mutation of the rhodopsin gene in one form of retinitis pigmentosa;Dryja;Nature,1990

2. A 3-bp deletion in the rhodopsin gene in a family with autosomal dominant retinitis pigmentosa;Inglehearn;Am. J. Hum. Genet.,1991

3. Autosomal dominant sectoral retinitis pigmentosa. Two families with transversion mutation incodon 23 of rhodopsin;Heckenlively;Arch. Ophthalmol.,1991

4. Ocular findings in patients with autosomal dominant retinitis pigmentosa and a rhodopsin gene defect (pro-23-his);Berson;Arch. Ophthalmol.,1991

5. Mutation spectrum of the rhodopsin gene among patients with autosomal dominant retinitis pigmentosa;Dryja;Proc. Natl. Acad. Sci. USA,1991

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