Retinitis Pigmentosa: Genes and Disease Mechanisms

Retinitis pigmentosa (RP) is a group of inherited disorders affecting 1 in 3000-7000 people and characterized by abnormalities of the photoreceptors (rods and cones) or the retinal pigment epithelium of the retina which lead to progressive visual loss. RP can be inherited in an autosomal dominant, a...

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Detalles Bibliográficos
Autores principales: Ferrari, Stefano, Di Iorio, Enzo, Barbaro, Vanessa, Ponzin, Diego, Sorrentino, Francesco S, Parmeggiani, Francesco
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bentham Science Publishers Ltd. 2011
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3131731/
https://www.ncbi.nlm.nih.gov/pubmed/22131869
http://dx.doi.org/10.2174/138920211795860107

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3131731/
https://www.ncbi.nlm.nih.gov/pubmed/22131869
http://dx.doi.org/10.2174/138920211795860107

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