Molecular Genetics of FAM161A in North American Patients with Early-Onset Retinitis Pigmentosa

Retinitis pigmentosa (RP) is a hereditary disease that leads to the progressive degeneration of retinal photoreceptor cells and to blindness. It is caused by mutations in several distinct genes, including the ciliary gene FAM161A, which is associated with a recessive form of this disorder. Recent in...

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Detalles Bibliográficos
Autores principales: Venturini, Giulia, Di Gioia, Silvio Alessandro, Harper, Shyana, Weigel-DiFranco, Carol, Rivolta, Carlo, Berson, Eliot L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3961368/
https://www.ncbi.nlm.nih.gov/pubmed/24651477
http://dx.doi.org/10.1371/journal.pone.0092479

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3961368/
https://www.ncbi.nlm.nih.gov/pubmed/24651477
http://dx.doi.org/10.1371/journal.pone.0092479

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