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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Detalles Bibliográficos
Autores principales: Chizzolini, Marzio, Galan, Alessandro, Milan, Elisabeth, Sebastiani, Adolfo, Costagliola, Ciro, 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/PMC3131733/
https://www.ncbi.nlm.nih.gov/pubmed/22131871
http://dx.doi.org/10.2174/138920211795860071

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3131733/
https://www.ncbi.nlm.nih.gov/pubmed/22131871
http://dx.doi.org/10.2174/138920211795860071

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