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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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Bibliografski detalji
Glavni autori: Chizzolini, Marzio, Galan, Alessandro, Milan, Elisabeth, Sebastiani, Adolfo, Costagliola, Ciro, Parmeggiani, Francesco
Format: Artigo
Jezik:Inglês
Izdano: Bentham Science Publishers Ltd 2011
Teme:
Online pristup: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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