Cell Ferroptosis: New Mechanism and New Hope for Retinitis Pigmentosa

Retinitis pigmentosa (RP) is a leading cause of inherited retinal degeneration, with more than 60 gene mutations. Despite the genetic heterogenicity, photoreceptor cell damage remains the hallmark of RP pathology. As a result, RP patients usually suffer from reduced night vision, loss of peripheral...

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Detalles Bibliográficos
Autores principales: Yang, Ming, So, Kwok-Fai, Lam, Wai-Ching, Lo, Amy Cheuk Yin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8393369/
https://www.ncbi.nlm.nih.gov/pubmed/34440922
http://dx.doi.org/10.3390/cells10082153

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8393369/
https://www.ncbi.nlm.nih.gov/pubmed/34440922
http://dx.doi.org/10.3390/cells10082153

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