CLINICAL PRESENTATION AND DISEASE COURSE OF USHER SYNDROME BECAUSE OF MUTATIONS IN MYO7A OR USH2A-Reference-Cited by-同舟云学术

CLINICAL PRESENTATION AND DISEASE COURSE OF USHER SYNDROME BECAUSE OF MUTATIONS IN MYO7A OR USH2A

Published:2017-08 Issue:8 Volume:37 Page:1581-1590
ISSN:0275-004X
Container-title:Retina
language:en
Short-container-title:

Author:

Testa Francesco,Melillo Paolo,Bonnet Crystel,Marcelli Vincenzo,de Benedictis Antonella,Colucci Raffaella,Gallo Beatrice,Kurtenbach Anne,Rossi Settimio,Marciano Elio,Auricchio Alberto,Petit Christine,Zrenner Eberhart,Simonelli Francesca

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Ophthalmology,General Medicine

Reference42 articles.

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4. Natural history and retinal structure in patients with Usher syndrome type 1 owing to MYO7A mutation;Lenassi;Ophthalmology,2014

5. Comprehensive molecular diagnosis of a large cohort of Japanese retinitis pigmentosa and Usher syndrome patients by next-generation sequencing;Oishi;Invest Ophthalmol Vis Sci,2014

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1. CDH23-Associated Usher Syndrome: Clinical Features, Retinal Imaging, and Natural History;Investigative Ophthalmology & Visual Science;2024-07-17

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