Mutation screening of multiple genes in Spanish patients with autosomal recessive retinitis pigmentosa by targeted resequencing.

Retinitis Pigmentosa (RP) is a heterogeneous group of inherited retinal dystrophies characterised ultimately by the loss of photoreceptor cells. RP is the leading cause of visual loss in individuals younger than 60 years, with a prevalence of about 1 in 4000. The molecular genetic diagnosis of autos...

Full description

Bibliographic Details
Main Authors: María González-del Pozo, Salud Borrego, Isabel Barragán, Juan I Pieras, Javier Santoyo, Nerea Matamala, Belén Naranjo, Joaquín Dopazo, Guillermo Antiñolo
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2011-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3229495?pdf=render