An Update on the Genetics of Usher Syndrome

Usher syndrome (USH) is an autosomal recessive disease characterized by hearing loss, retinitis pigmentosa (RP), and, in some cases, vestibular dysfunction. It is clinically and genetically heterogeneous and is the most common cause underlying deafness and blindness of genetic origin. Clinically, US...

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Detalles Bibliográficos
Autores principales: Millán, José M., Aller, Elena, Jaijo, Teresa, Blanco-Kelly, Fiona, Gimenez-Pardo, Ascensión, Ayuso, Carmen
Formato: Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2011
Materias:
Review Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3017948/
https://www.ncbi.nlm.nih.gov/pubmed/21234346
http://dx.doi.org/10.1155/2011/417217

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3017948/
https://www.ncbi.nlm.nih.gov/pubmed/21234346
http://dx.doi.org/10.1155/2011/417217

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