Sparing gene therapy for Inherited ROd COne dystrophies

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Metabolic and Redox Signaling of the Nucleoredoxin-Like-1 Gene for the Treatment of Genetic Retinal Diseases

Autores: Emmanuelle Clérin, Myriam Marussig, José-Alain Sahel, Thierry Léveillard
Publicado en: International Journal of Molecular Sciences, Edición 21/5, 2020, Página(s) 1625, ISSN 1422-0067
Editor: Multidisciplinary Digital Publishing Institute (MDPI)
DOI: 10.3390/ijms21051625

Natural history of retinitis pigmentosa due to RHO, PDE6A OR PDE6B mutations

Autores: Myriam Marussig, Léa Thiebault, Pierre-Axel Vinot, Berthe Pom, Camille Andrieu, Christina Zeitz, Thierry D Leveillard, Florence Allouche, Saddek Mohand-Said, Isabelle S Audo, Jose Alain Sahe
Publicado en: Investigative Ophthalmology & Visual Science (IOVS), Edición June 2020, Volume 61, Edición 7, 2020, ISSN 0146-0404
Editor: Association for Research in Vision and Ophthalmology

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