AAV-Mediated Clarin-1 Expression in the Mouse Retina: Implications for USH3A Gene Therapy-Reference-Cited by-同舟云学术

AAV-Mediated Clarin-1 Expression in the Mouse Retina: Implications for USH3A Gene Therapy

Published:2016-02-16 Issue:2 Volume:11 Page:e0148874
ISSN:1932-6203
Container-title:PLOS ONE
language:en
Short-container-title:PLoS ONE

Author:

Dinculescu Astra,Stupay Rachel M.,Deng Wen-Tao,Dyka Frank M.,Min Seok-Hong,Boye Sanford L.,Chiodo Vince A.,Abrahan Carolina E.,Zhu Ping,Li Qiuhong,Strettoi Enrica,Novelli Elena,Nagel-Wolfrum Kerstin,Wolfrum Uwe,Smith W. Clay,Hauswirth William W.

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

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1. Retinal Phenotype of Patients with CLRN1-Associated Usher 3A Syndrome in French Light4Deaf Cohort;Investigative Opthalmology & Visual Science;2022-04-28

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3. Retinal Gene Therapy for Usher Syndrome: Current Developments, Challenges, and Perspectives;International Ophthalmology Clinics;2021

4. Usher Syndrome: Genetics and Molecular Links of Hearing Loss and Directions for Therapy;Frontiers in Genetics;2020-10-22

5. A Review of Gene, Drug and Cell-Based Therapies for Usher Syndrome;Frontiers in Cellular Neuroscience;2020-07-09