Unravelling the genetic basis of simplex Retinitis Pigmentosa cases

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), autosomal recessive (ar) and X-linked (xl) disorder....

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Detalles Bibliográficos
Autores principales: Bravo-Gil, Nereida, González-del Pozo, María, Martín-Sánchez, Marta, Méndez-Vidal, Cristina, Rodríguez-de la Rúa, Enrique, Borrego, Salud, Antiñolo, Guillermo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5291209/
https://www.ncbi.nlm.nih.gov/pubmed/28157192
http://dx.doi.org/10.1038/srep41937

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5291209/
https://www.ncbi.nlm.nih.gov/pubmed/28157192
http://dx.doi.org/10.1038/srep41937

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