Double Hyperautofluorescent Rings in Patients with USH2A-Retinopathy

USH2A mutation is the most common cause of retinitis pigmentosa, with or without hearing impairment. Patients most commonly exhibit hyperautofluorescent ring on fundus autofluorescence imaging (FAF) and rod-cone dystrophy on electrophysiology. A detailed study of three USH2A patients with a rare pat...

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Detalles Bibliográficos
Autores principales: Fakin, Ana, Šuštar, Maja, Brecelj, Jelka, Bonnet, Crystel, Petit, Christine, Zupan, Andrej, Glavač, Damjan, Jarc-Vidmar, Martina, Battelino, Saba, Hawlina, Marko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6947471/
https://www.ncbi.nlm.nih.gov/pubmed/31766479
http://dx.doi.org/10.3390/genes10120956

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6947471/
https://www.ncbi.nlm.nih.gov/pubmed/31766479
http://dx.doi.org/10.3390/genes10120956

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