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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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Autores principales: Ferrari, Stefano, Di Iorio, Enzo, Barbaro, Vanessa, Ponzin, Diego, Sorrentino, Francesco S, Parmeggiani, Francesco
Formato: Artigo
Lenguaje:Inglês
Publicado: Bentham Science Publishers Ltd. 2011
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Acceso en línea: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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