A novel locus for autosomal dominant non-syndromic deafness (DFNA41) maps to chromosome 12q24-qter
A novel locus for autosomal dominant non-syndromic deafness (DFNA41) maps to chromosome 12q24-qter
About this item
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Author / Creator
Blanton, S H , Liang, C Y , Cai, M W , Pandya, A , Du, L L , Landa, B , Mummalanni, S , Li, K S , Chen, Z Y , Qin, X N , Liu, Y F , Balkany, T , Nance, W E and Liu, X Z
Publisher
London: BMJ Publishing Group Ltd
Journal title
Language
English
Formats
Publication information
Publisher
London: BMJ Publishing Group Ltd
Subjects
More information
Scope and Contents
Contents
We have studied 36 subjects in a large multigenerational Chinese family that is segregating for an autosomal dominant adult onset form of progressive non-syndromic hearing loss. All affected subjects had bilateral sensorineural hearing loss involving all frequencies with some significant gender differences in initial presentation. After excluding l...
Alternative Titles
Full title
A novel locus for autosomal dominant non-syndromic deafness (DFNA41) maps to chromosome 12q24-qter
Authors, Artists and Contributors
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Primary Identifiers
Record Identifier
TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_1735215
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_1735215
Other Identifiers
ISSN
0022-2593,1468-6244
E-ISSN
1468-6244
DOI
10.1136/jmg.39.8.567
