Massively Parallel DNA Sequencing Successfully Identifies New Causative Mutations in Deafness Genes in Patients with Cochlear Implantation and EAS

Genetic factors, the most common etiology in severe to profound hearing loss, are one of the key determinants of Cochlear Implantation (CI) and Electric Acoustic Stimulation (EAS) outcomes. Satisfactory auditory performance after receiving a CI/EAS in patients with certain deafness gene mutations in...

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Detalles Bibliográficos
Autores principales: Miyagawa, Maiko, Nishio, Shin-ya, Ikeda, Takuo, Fukushima, Kunihiro, Usami, Shin-ichi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3794008/
https://www.ncbi.nlm.nih.gov/pubmed/24130743
http://dx.doi.org/10.1371/journal.pone.0075793

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3794008/
https://www.ncbi.nlm.nih.gov/pubmed/24130743
http://dx.doi.org/10.1371/journal.pone.0075793

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