Genetic analysis of Tunisian families with Usher syndrome type 1: toward improving early molecular diagnosis

PURPOSE: Usher syndrome accounts for about 50% of all hereditary deaf-blindness cases. The most severe form of this syndrome, Usher syndrome type I (USH1), is characterized by profound congenital sensorineural deafness, vestibular dysfunction, and retinitis pigmentosa. Six USH1 genes have been ident...

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Detalles Bibliográficos
Autores principales: Ben-Rebeh, Imen, Grati, Mhamed, Bonnet, Crystel, Bouassida, Walid, Hadjamor, Imen, Ayadi, Hammadi, Ghorbel, Abdelmonem, Petit, Christine, Masmoudi, Saber
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Vision 2016
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4950652/
https://www.ncbi.nlm.nih.gov/pubmed/27440999

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4950652/
https://www.ncbi.nlm.nih.gov/pubmed/27440999

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