The Potential Role of Epigenetic Mechanisms in the Development of Retinitis Pigmentosa and Related Photoreceptor Dystrophies

Retinitis pigmentosa and related photoreceptor dystrophies (RPRPD) are rare retinal diseases caused by hereditary gene mutations resulting in photoreceptor death, followed by vision loss. While numerous genes involved in these diseases have been identified, many cases have still not been associated...

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Detalles Bibliográficos
Autores principales: Dvoriantchikova, Galina, Lypka, Karin Rose, Ivanov, Dmitry
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8961674/
https://www.ncbi.nlm.nih.gov/pubmed/35360866
http://dx.doi.org/10.3389/fgene.2022.827274

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8961674/
https://www.ncbi.nlm.nih.gov/pubmed/35360866
http://dx.doi.org/10.3389/fgene.2022.827274

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