Gene panel sequencing in Brazilian patients with retinitis pigmentosa

BACKGROUND: Retinal dystrophies constitute a group of diseases characterized by clinical variability and pronounced genetic heterogeneity. Retinitis pigmentosa is the most common subtype of hereditary retinal dystrophy and is characterized by a progressive loss of peripheral field vision (Tunnel Vis...

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Detalles Bibliográficos
Autores principales: Costa, Kárita Antunes, Salles, Mariana Vallim, Whitebirch, Chris, Chiang, John, Sallum, Juliana Maria Ferraz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5592712/
https://www.ncbi.nlm.nih.gov/pubmed/28912962
http://dx.doi.org/10.1186/s40942-017-0087-6

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5592712/
https://www.ncbi.nlm.nih.gov/pubmed/28912962
http://dx.doi.org/10.1186/s40942-017-0087-6

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