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Social Health Insurance-Based Simultaneous Screening for 154 Mutations in 19 Deafness Genes Efficien...

Social Health Insurance-Based Simultaneous Screening for 154 Mutations in 19 Deafness Genes Efficien...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_plos_journals_1819428178

Social Health Insurance-Based Simultaneous Screening for 154 Mutations in 19 Deafness Genes Efficiently Identified Causative Mutations in Japanese Hearing Loss Patients

About this item

Full title

Social Health Insurance-Based Simultaneous Screening for 154 Mutations in 19 Deafness Genes Efficiently Identified Causative Mutations in Japanese Hearing Loss Patients

Publisher

United States: Public Library of Science

Journal title

PloS one, 2016-09, Vol.11 (9), p.e0162230-e0162230

Language

English

Formats

Publication information

Publisher

United States: Public Library of Science

More information

Scope and Contents

Contents

Sensorineural hearing loss is one of the most common neurosensory disorders in humans. The incidence of SNHL is estimated to be 1 in 500-1000 newborns. In more than half of these patients, the hearing loss is associated with genetic causes. In Japan, genetic testing for the patients with SNHL using the Invader assay to screen for 46 mutations in 13...

Alternative Titles

Full title

Social Health Insurance-Based Simultaneous Screening for 154 Mutations in 19 Deafness Genes Efficiently Identified Causative Mutations in Japanese Hearing Loss Patients

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_plos_journals_1819428178

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_plos_journals_1819428178

Other Identifiers

ISSN

1932-6203

E-ISSN

1932-6203

DOI

10.1371/journal.pone.0162230

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