Late-onset non-syndromic hearing impairment is the most common type of neurological dysfunction in the elderly. It can be either acquired or inherited, although the relative impact of heredity on this type of loss is not known. To date, nine different genes have been localized, but none has been cloned. Using an extended American family in which a gene for autosomal dominant late-onset non-syndromic hearing impairment is segregating, we have identified a new locus, DFNA10, on chromosome 6.
|Original language||English (US)|
|Number of pages||4|
|Journal||Human Molecular Genetics|
|State||Published - Jun 1996|
ASJC Scopus subject areas
- Molecular Biology