Defining Outcomes for Clinical Trials of Leber Congenital Amaurosis Caused by GUCY2D Mutations-Reference-Cited by-同舟云学术

Defining Outcomes for Clinical Trials of Leber Congenital Amaurosis Caused by GUCY2D Mutations

Published:2017-05 Issue: Volume:177 Page:44-57
ISSN:0002-9394
Container-title:American Journal of Ophthalmology
language:en
Short-container-title:American Journal of Ophthalmology

Author:

Jacobson Samuel G.,Cideciyan Artur V.,Sumaroka Alexander,Roman Alejandro J.,Charng Jason^ORCID,Lu Monica^ORCID,Choudhury Shreyasi,Schwartz Sharon B.,Heon Elise,Fishman Gerald A.,Boye Shannon E.

Publisher

Elsevier BV

Subject

Ophthalmology

Reference82 articles.

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2. Review and update on the molecular basis of Leber congenital amaurosis;Chacon-Camacho;World J Clin Cases,2015

3. Leber congenital amaurosis: genotypes and retinal structure phenotypes;Jacobson;Adv Exp Med Biol,2016

4. Leber congenital amaurosis due to RPE65 mutations and its treatment with gene therapy;Cideciyan;Prog Retin Eye Res,2010

5. A mini-review: animal models of GUCY2D Leber congenital amaurosis (LCA1);Boye;Adv Exp Biol,2016

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