TY  - JOUR
AU  - González-del Pozo, María E.
AU  - Borrego, Salud
AU  - Barragán, Isabel
AU  - Pieras, Juan I
AU  - Santoyo, Javier
AU  - Matamala, Nerea
AU  - Naranjo, Belén
AU  - Dopazo, Joaquín
AU  - Antiñolo, Guillermo
PY  - 2011
DO  - 10.1371/journal.pone.0027894
UR  - http://hdl.handle.net/10668/397
T2  - PLoS One
AB  - 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...
LA  - en
PB  - PLoS
KW  - Retinitis Pigmentosa
KW  - España
KW  - Análisis de Micromatrices
KW  - Medical Subject Headings::Diseases::Congenital, Hereditary, and Neonatal Diseases and Abnormalities::Genetic Diseases, Inborn::Eye Diseases, Hereditary::Retinitis Pigmentosa
KW  - Medical Subject Headings::Analytical, Diagnostic and Therapeutic Techniques and Equipment::Investigative Techniques::Chemistry Techniques, Analytical::Microchip Analytical Procedures::Microarray Analysis
KW  - Medical Subject Headings::Geographicals
KW  - Medical Subject Headings::Geographicals::Geographic Locations::Europe::Spain
TI  - Mutation screening of multiple genes in Spanish patients with autosomal recessive retinitis pigmentosa by targeted resequencing.
TY  - research article
ER  -