Molecular investigation in children candidates and submitted to cochlear implantation

AIM: recent progresses in molecular biology have been made in the diagnosis of sensorineural hearing loss. The high prevalence of a connexin 26 gene mutation, and its easy identification have made the diagnosis possible. The most frequent gene mutation is called 35delG. The purpose of this study was...

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Detalles Bibliográficos
Autores principales: Bernardes, Raquel, Bortoncello, Silvana, Christiani, Thalita Vitachi, Sartorato, Edi Lúcia, e Silva, Rodrigo César, Porto, Paulo R. Cantanhede
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2015
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9443549/
https://www.ncbi.nlm.nih.gov/pubmed/17119768
http://dx.doi.org/10.1016/S1808-8694(15)30965-4

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9443549/
https://www.ncbi.nlm.nih.gov/pubmed/17119768
http://dx.doi.org/10.1016/S1808-8694(15)30965-4

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