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Massively parallel DNA sequencing successfully identifies new causative mutations in deafness genes...

Massively parallel DNA sequencing successfully identifies new causative mutations in deafness genes...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_plos_journals_1440829708

Massively parallel DNA sequencing successfully identifies new causative mutations in deafness genes in patients with cochlear implantation and EAS

About this item

Full title

Massively parallel DNA sequencing successfully identifies new causative mutations in deafness genes in patients with cochlear implantation and EAS

Publisher

United States: Public Library of Science

Journal title

PloS one, 2013-10, Vol.8 (10), p.e75793-e75793

Language

English

Formats

Publication information

Publisher

United States: Public Library of Science

More information

Scope and Contents

Contents

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...

Alternative Titles

Full title

Massively parallel DNA sequencing successfully identifies new causative mutations in deafness genes in patients with cochlear implantation and EAS

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_plos_journals_1440829708

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_plos_journals_1440829708

Other Identifiers

ISSN

1932-6203

E-ISSN

1932-6203

DOI

10.1371/journal.pone.0075793

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