SD-OCT imaging as a valuable tool to support molecular genetic diagnostics of Usher syndrome type 1
Author:
Publisher
Elsevier BV
Subject
Ophthalmology,Pediatrics, Perinatology, and Child Health
Reference13 articles.
1. Usher syndrome: hearing loss, retinal degeneration and associated abnormalities;Mathur;Biochim Biophys Acta,2015
2. An innovative strategy for the molecular diagnosis of Usher syndrome identifies causal biallelic mutations in 93% of European patients;Bonnet;Eur J Hum Genet,2016
3. Clinical presentation and disease course of Usher syndrome because of mutations in MYO7A or USH2A;Testa;Retina,2017
4. Comprehensive sequence analysis of nine Usher syndrome genes in the UK National Collaborative Usher Study;Le Quesne Stabej;J Med Genet,2012
5. Usher syndrome type III can mimic other types of Usher syndrome;Pennings;Ann Otol Rhinol Laryngol,2003
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