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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Hlavní autoři: Miyagawa, Maiko, Nishio, Shin-ya, Ikeda, Takuo, Fukushima, Kunihiro, Usami, Shin-ichi
Médium: Artigo
Jazyk:Inglês
Vydáno: Public Library of Science 2013
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Research Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC3794008/
https://ncbi.nlm.nih.gov/pubmed/24130743
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0075793
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