Spectrum of Mutations in the RPGR Gene That Are Identified in 20% of Families with X-Linked Retinitis Pigmentosa-Reference-Cited by-同舟云学术

Spectrum of Mutations in the RPGR Gene That Are Identified in 20% of Families with X-Linked Retinitis Pigmentosa

Published:1997-12 Issue:6 Volume:61 Page:1287-1292
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Buraczynska Monika,Wu Weiping,Fujita Ricardo,Buraczynska Kinga,Phelps Ellen,Andréasson Sten,Bennett Jean,Birch David G.,Fishman Gerald A.,Hoffman Dennis R.,Inana George,Jacobson Samuel G.,Musarella Maria A.,Sieving Paul A.,Swaroop Anand

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference19 articles.

1. Update on nomenclature for mutations;Ad Hoc Committee on Mutation Nomenclature;Hum Mutat,1996

2. X-linked retinitis pigmentosa;Aldred,1994

3. Phenotypes in three Swedish families with X-linked retinitis pigmentosa caused by different mutations in the RPGR gene;Andréasson;Am J Ophthalmol,1997

4. X-linked retinitis pigmentosa;Bird;Br J Ophthalmol,1975

5. Mutation spectrum of the RPGR gene in X-linked retinitis pigmentosa;Bruns;Invest Ophthalmol Vis Sci,1997

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