Abstract
Inherited hearing impairment can occur either in the presence of other clinical features (syndromic hearing loss, SHL) or in isolation (non-syndromic hearing loss, NSHL). The latter is more common and is highly heterogeneous. To date, six NSHL loci have been mapped. We report the identification of a seventh locus (DFNA4) on chromosome 19q13 and suggest DM kinase as a possible candidate gene.
Original language | English (US) |
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Pages (from-to) | 1073-1076 |
Number of pages | 4 |
Journal | Human Molecular Genetics |
Volume | 4 |
Issue number | 6 |
DOIs | |
State | Published - Jun 1995 |
Externally published | Yes |
ASJC Scopus subject areas
- Molecular Biology
- Genetics
- Genetics(clinical)