Carrier frequency of GJB2 gene mutations c.35delG, c.235delC and c.167delT among the populations of...
Carrier frequency of GJB2 gene mutations c.35delG, c.235delC and c.167delT among the populations of Eurasia
About this item
Full title
Author / Creator
Publisher
London: Nature Publishing Group UK
Journal title
Language
English
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Publication information
Publisher
London: Nature Publishing Group UK
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Scope and Contents
Contents
Hearing impairment is one of the most common disorders of sensorineural function and the incidence of profound prelingual deafness is about 1 per 1000 at birth.
GJB2
gene mutations make the largest contribution to hereditary hearing impairment. The spectrum and prevalence of some
GJB2
mutations are known to be dependent on the ethnic or...
Alternative Titles
Full title
Carrier frequency of GJB2 gene mutations c.35delG, c.235delC and c.167delT among the populations of Eurasia
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TN_cdi_proquest_miscellaneous_814463025
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_814463025
Other Identifiers
ISSN
1434-5161
E-ISSN
1435-232X
DOI
10.1038/jhg.2010.101
