Molecular epidemiology of Usher syndrome in Italy

PURPOSE: Usher syndrome is an autosomal recessive disorder characterized by hearing and vision loss. Usher syndrome is divided into three clinical subclasses (type 1, type 2, and type 3), which differ in terms of the severity and progression of hearing loss and the presence or absence of vestibular...

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Detalles Bibliográficos
Autores principales: Vozzi, Diego, Aaspõllu, Anu, Athanasakis, Emmanouil, Berto, Anna, Fabretto, Antonella, Licastro, Danilo, Külm, Maigi, Testa, Francesco, Trevisi, Patrizia, Vahter, Marju, Ziviello, Carmela, Martini, Alessandro, Simonelli, Francesca, Banfi, Sandro, Gasparini, Paolo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Vision 2011
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3130723/
https://www.ncbi.nlm.nih.gov/pubmed/21738395

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3130723/
https://www.ncbi.nlm.nih.gov/pubmed/21738395

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