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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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Bibliografski detalji
Glavni autori: Miyagawa, Maiko, Nishio, Shin-ya, Ikeda, Takuo, Fukushima, Kunihiro, Usami, Shin-ichi
Format: Artigo
Jezik:Inglês
Izdano: Public Library of Science 2013
Teme:
Online pristup: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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