Correlation between audiometric data and the 35delG mutation in ten patients

Mutations in the connexin 26 gene seem to be extremely common in non-syndromic hereditary deafness genesis, especially the 35delG, but there are still only a few studies that describe the audiometric characteristics of patients with these mutations. AIM: to analyze the audiometric characteristics of...

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Detalles Bibliográficos
Autores principales: Belintani Piatto, Vânia, Vasques Moreira, Otávio Augusto, Orate Menezes da Silva, Magali Aparecida, Victor Maniglia, José, Coimbra Pereira, Márcio, Sartorato, Edi Lúcia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2015
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9450577/
https://www.ncbi.nlm.nih.gov/pubmed/18278224
http://dx.doi.org/10.1016/S1808-8694(15)31174-5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9450577/
https://www.ncbi.nlm.nih.gov/pubmed/18278224
http://dx.doi.org/10.1016/S1808-8694(15)31174-5

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