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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...
| Autores principales: | , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Elsevier
2015
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| Materias: | |
| 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 |