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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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Detalhes bibliográficos
Main Authors: Ferrari, Stefano, Di Iorio, Enzo, Barbaro, Vanessa, Ponzin, Diego, Sorrentino, Francesco S, Parmeggiani, Francesco
Formato: Artigo
Idioma:Inglês
Publicado em: Bentham Science Publishers Ltd. 2011
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3131731/
https://ncbi.nlm.nih.gov/pubmed/22131869
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2174/138920211795860107
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