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. 1995 Jun;4(6):1073-6.
doi: 10.1093/hmg/4.6.1073.

Linkage of a gene for dominant non-syndromic deafness to chromosome 19

A H Chen  1 , L Ni, K Fukushima, J Marietta, M O'Neill, P Coucke, P Willems, R J Smith
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Linkage of a gene for dominant non-syndromic deafness to chromosome 19

A H Chen et al. Hum Mol Genet. 1995 Jun.

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.

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