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Good Epidemiologic Practice in Retinitis Pigmentosa: From Phenotyping to Biobanking

Inherited retinal dystrophies, such as retinitis pigmentosa (RP), include a group of relatively rare hereditary diseases caused by mutations in genes that code for proteins involved in the maintenance and function of the photoreceptor cells (cones and rods). The different forms of RP consist of prog...

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Detalhes bibliográficos
Main Authors: Chizzolini, Marzio, Galan, Alessandro, Milan, Elisabeth, Sebastiani, Adolfo, Costagliola, Ciro, Parmeggiani, Francesco
Formato: Artigo
Idioma:Inglês
Publicado em: Bentham Science Publishers Ltd 2011
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3131733/
https://ncbi.nlm.nih.gov/pubmed/22131871
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2174/138920211795860071
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