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GJB2 mutation spectrum in 2063 Chinese patients with nonsyndromic hearing impairment

GJB2 mutation spectrum in 2063 Chinese patients with nonsyndromic hearing impairment

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_05c6bc3b9b4e41d4b1f10e2d89c19cae

GJB2 mutation spectrum in 2063 Chinese patients with nonsyndromic hearing impairment

About this item

Full title

GJB2 mutation spectrum in 2063 Chinese patients with nonsyndromic hearing impairment

Publisher

BioMed Central Ltd

Journal title

Journal of translational medicine, 2009-04, Vol.7 (26), p.26-26, Article 26

Language

English

Formats

Publication information

Publisher

BioMed Central Ltd

More information

Scope and Contents

Contents

Background Mutations in GJB2 are the most common molecular defects responsible for autosomal recessive nonsyndromic hearing impairment (NSHI). The mutation spectra of this gene vary among different ethnic groups. Methods In order to understand the spectrum and frequency of GJB2 mutations in the Chinese population, the coding region of the GJB2 gene...

Alternative Titles

Full title

GJB2 mutation spectrum in 2063 Chinese patients with nonsyndromic hearing impairment

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Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_05c6bc3b9b4e41d4b1f10e2d89c19cae

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_05c6bc3b9b4e41d4b1f10e2d89c19cae

Other Identifiers

ISSN

1479-5876

E-ISSN

1479-5876

DOI

10.1186/1479-5876-7-26

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