Massively parallel DNA sequencing successfully identifies new causative mutations in deafness genes...
Massively parallel DNA sequencing successfully identifies new causative mutations in deafness genes in patients with cochlear implantation and EAS
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United States: Public Library of Science
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English
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United States: Public Library of Science
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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 indicates that genetic testing would be helpful in p...
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Massively parallel DNA sequencing successfully identifies new causative mutations in deafness genes in patients with cochlear implantation and EAS
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TN_cdi_plos_journals_1440829708
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https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_plos_journals_1440829708
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ISSN
1932-6203
E-ISSN
1932-6203
DOI
10.1371/journal.pone.0075793