Deafness Genes in Israel: Implications for Diagnostics in the Clinic
Deafness Genes in Israel: Implications for Diagnostics in the Clinic
About this item
Full title
Author / Creator
Publisher
New York: Nature Publishing Group US
Journal title
Language
English
Formats
Publication information
Publisher
New York: Nature Publishing Group US
Subjects
More information
Scope and Contents
Contents
The identification of the molecular basis of deafness in the last decade has made a remarkable impact on genetic counseling and diagnostics for the hearing impaired population. Since the discovery of the most prevalent form of deafness associated with mutations in the
GJB2
(connexin 26) gene, many other genes have been found worldwide, with a...
Alternative Titles
Full title
Deafness Genes in Israel: Implications for Diagnostics in the Clinic
Authors, Artists and Contributors
Author / Creator
Identifiers
Primary Identifiers
Record Identifier
TN_cdi_proquest_miscellaneous_67510556
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_67510556
Other Identifiers
ISSN
0031-3998
E-ISSN
1530-0447
DOI
10.1203/PDR.0b013e3181aabd7f
