A novel mutation within the MIR96 gene causes non-syndromic inherited hearing loss in an Italian family by altering pre-miRNA processing

The miR-96, miR-182 and miR-183 microRNA (miRNA) family is essential for differentiation and function of the vertebrate inner ear. Recently, point mutations within the seed region of miR-96 were reported in two Spanish families with autosomal dominant non-syndromic sensorineural hearing loss (NSHL)...

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Detalles Bibliográficos
Autores principales: Soldà, Giulia, Robusto, Michela, Primignani, Paola, Castorina, Pierangela, Benzoni, Elena, Cesarani, Antonio, Ambrosetti, Umberto, Asselta, Rosanna, Duga, Stefano
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2012
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3259013/
https://www.ncbi.nlm.nih.gov/pubmed/22038834
http://dx.doi.org/10.1093/hmg/ddr493

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3259013/
https://www.ncbi.nlm.nih.gov/pubmed/22038834
http://dx.doi.org/10.1093/hmg/ddr493

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