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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Bibliografiske detaljer
Udgivet i:Genes (Basel)
Main Authors: Fakin, Ana, Šuštar, Maja, Brecelj, Jelka, Bonnet, Crystel, Petit, Christine, Zupan, Andrej, Glavač, Damjan, Jarc-Vidmar, Martina, Battelino, Saba, Hawlina, Marko
Format: Artigo
Sprog:Inglês
Udgivet: MDPI 2019
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Article
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC6947471/
https://ncbi.nlm.nih.gov/pubmed/31766479
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/genes10120956
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