Substantial restoration of night vision in adult mice with congenital stationary night blindness

Complete congenital stationary night blindness (cCSNB) due to mutations in TRPM1, GRM6, GPR179, NYX, or leucine-rich repeat immunoglobulin-like transmembrane domain 3 (LRIT3) is an incurable inherited retinal disorder characterized by an ON-bipolar cell (ON-BC) defect. Since the disease is non-degen...

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Detalles Bibliográficos
Autores principales: Varin, Juliette, Bouzidi, Nassima, Gauvain, Gregory, Joffrois, Corentin, Desrosiers, Melissa, Robert, Camille, De Sousa Dias, Miguel Miranda, Neuillé, Marion, Michiels, Christelle, Nassisi, Marco, Sahel, José-Alain, Picaud, Serge, Audo, Isabelle, Dalkara, Deniz, Zeitz, Christina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society of Gene & Cell Therapy 2021
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8339357/
https://www.ncbi.nlm.nih.gov/pubmed/34401402
http://dx.doi.org/10.1016/j.omtm.2021.05.008

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