Depleted Calcium Stores and Increased Calcium Entry in Rod Photoreceptors of the Cacna2d4 Mouse Model of Cone-Rod Dystrophy RCD4

Unidentified pathogenetic mechanisms and genetic and clinical heterogeneity represent critical factors hindering the development of treatments for inherited retinal dystrophies. Frameshift mutations in Cacna2d4, which codes for an accessory subunit of voltage-gated calcium channels (VGCC), cause con...

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Detalles Bibliográficos
Autores principales: Vellani, Vittorio, Mauro, Giovanna, Demontis, Gian Carlo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9656469/
https://www.ncbi.nlm.nih.gov/pubmed/36361866
http://dx.doi.org/10.3390/ijms232113080

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9656469/
https://www.ncbi.nlm.nih.gov/pubmed/36361866
http://dx.doi.org/10.3390/ijms232113080

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