TY  - JOUR
AU  - Bravo-Gil, Nereida
AU  - González-Del Pozo, María
AU  - Martín-Sánchez, Marta
AU  - Méndez-Vidal, Cristina
AU  - Rodríguez-de la Rúa, Enrique
AU  - Borrego, Salud
AU  - Antiñolo, Guillermo
PY  - 2017
DO  - 10.1038/srep41937
UR  - http://hdl.handle.net/10668/10833
T2  - Scientific reports
AB  - Retinitis Pigmentosa (RP) is the most common form of inherited retinal dystrophy (IRD) characterized ultimately by photoreceptors degeneration. Exhibiting great clinical and genetic heterogeneity, RP can be inherited as an autosomal dominant (ad),...
LA  - en
KW  - Female
KW  - Genetic Loci
KW  - Genetic Predisposition to Disease
KW  - Genome-Wide Association Study
KW  - Humans
KW  - Male
KW  - Pedigree
KW  - Retinitis Pigmentosa
TI  - Unravelling the genetic basis of simplex Retinitis Pigmentosa cases.
TY  - research article
VL  - 7
ER  -