CERKL, a Retinal Dystrophy Gene, Regulates Mitochondrial Transport and Dynamics in Hippocampal Neurons

Mutations in the Ceramide Kinase-like (CERKL) gene cause retinal dystrophies, characterized by progressive degeneration of retinal neurons, which eventually lead to vision loss. Among other functions, CERKL is involved in the regulation of autophagy, mitochondrial dynamics, and metabolism in the ret...

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Detalles Bibliográficos
Autores principales: García-Arroyo, Rocío, Marfany, Gemma, Mirra, Serena
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9570143/
https://www.ncbi.nlm.nih.gov/pubmed/36232896
http://dx.doi.org/10.3390/ijms231911593

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9570143/
https://www.ncbi.nlm.nih.gov/pubmed/36232896
http://dx.doi.org/10.3390/ijms231911593

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