Mutational screening of the USH2A gene in Spanish USH patients reveals 23 novel pathogenic mutations

BACKGROUND: Usher Syndrome type II (USH2) is an autosomal recessive disorder, characterized by moderate to severe hearing impairment and retinitis pigmentosa (RP). Among the three genes implicated, mutations in the USH2A gene account for 74-90% of the USH2 cases. METHODS: To identify the genetic cau...

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Detalles Bibliográficos
Autores principales: Garcia-Garcia, Gema, Aparisi, Maria J, Jaijo, Teresa, Rodrigo, Regina, Leon, Ana M, Avila-Fernandez, Almudena, Blanco-Kelly, Fiona, Bernal, Sara, Navarro, Rafael, Diaz-Llopis, Manuel, Baiget, Montserrat, Ayuso, Carmen, Millan, Jose M, Aller, Elena
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3207874/
https://www.ncbi.nlm.nih.gov/pubmed/22004887
http://dx.doi.org/10.1186/1750-1172-6-65

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3207874/
https://www.ncbi.nlm.nih.gov/pubmed/22004887
http://dx.doi.org/10.1186/1750-1172-6-65

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