Mutations in Cdh23, encoding a new type of cadherin, cause stereocilia disorganization in waltzer, t...
Mutations in Cdh23, encoding a new type of cadherin, cause stereocilia disorganization in waltzer, the mouse model for Usher syndrome type 1D
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
Mouse chromosome 10 harbors several loci associated with hearing loss, including waltzer (
v
), modifier-of deaf waddler (
mdfw
) and Age-related hearing loss
1
(
Ahl
). The human region that is orthologous to the mouse 'waltzer' region is located at 10q21–q22 and contains the human deafness loci
DFNB12
and
USH1D
Alternative Titles
Full title
Mutations in Cdh23, encoding a new type of cadherin, cause stereocilia disorganization in waltzer, the mouse model for Usher syndrome type 1D
Authors, Artists and Contributors
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Primary Identifiers
Record Identifier
TN_cdi_proquest_miscellaneous_877597507
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_877597507
Other Identifiers
ISSN
1061-4036
E-ISSN
1546-1718
DOI
10.1038/83660
