Leber Congenital Amaurosis Associated with AIPL1: Challenges in Ascribing Disease Causation, Clinical Findings, and Implications for Gene Therapy-Reference-Cited by-同舟云学术

Leber Congenital Amaurosis Associated with AIPL1: Challenges in Ascribing Disease Causation, Clinical Findings, and Implications for Gene Therapy

Published:2012-03-06 Issue:3 Volume:7 Page:e32330
ISSN:1932-6203
Container-title:PLoS ONE
language:en
Short-container-title:PLoS ONE

Author:

Tan Mei Hong,Mackay Donna S.,Cowing Jill,Tran Hoai Viet,Smith Alexander J.,Wright Genevieve A.,Dev-Borman Arundhati,Henderson Robert H.,Moradi Phillip,Russell-Eggitt Isabelle,MacLaren Robert E.,Robson Anthony G.,Cheetham Michael E.,Thompson Dorothy A.,Webster Andrew R.,Michaelides Michel,Ali Robin R.,Moore Anthony T.

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

Reference38 articles.

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2. Leber congenital amaurosis.;RG Weleber,2010

3. Effect of gene therapy on visual function in Leber's congenital amaurosis.;JW Bainbridge;N Engl J Med,2008

4. Human gene therapy for RPE65 isomerase deficiency activates the retinoid cycle of vision but with slow rod kinetics.;AV Cideciyan;Proc Natl Acad Sci U S A,2008

5. Safety and efficacy of gene transfer for Leber's congenital amaurosis.;AM Maguire;N Engl J Med,2008

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