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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Bibliographic Details
Main Authors: Millán, José M., Aller, Elena, Jaijo, Teresa, Blanco-Kelly, Fiona, Gimenez-Pardo, Ascensión, Ayuso, Carmen
Format: Artigo
Language:Inglês
Published: Hindawi Publishing Corporation 2011
Subjects:
Review Article
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC3017948/
https://ncbi.nlm.nih.gov/pubmed/21234346
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2011/417217
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