USH2A-retinopathy: From genetics to therapeutics
Author:
Funder
Wellcome Trust
Publisher
Elsevier BV
Subject
Cellular and Molecular Neuroscience,Sensory Systems,Ophthalmology
Reference137 articles.
1. Audiological findings in 100 USH2 patients;Abadie;Clin. Genet.,2012
2. Usherin, the defective protein in Usher syndrome type IIA, is likely to be a component of interstereocilia ankle links in the inner ear sensory cells;Adato;Hum. Mol. Genet.,2005
3. Inframe deletion of human ESPN is associated with deafness, vestibulopathy and vision impairment;Ahmed;J. Med. Genet.,2018
4. The USH2A c.2299delG mutation: dating its common origin in a Southern European population;Aller;Eur. J. Hum. Genet.,2010
5. Leveraging zebrafish to study retinal degenerations;Angueyra;Front. Cell Dev. Biol.,2018
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