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Article

A second family with nonsyndromic sensorineural hearing loss linked to Xp21.2: refinement of the DFN4 locus within DMD.

Genomics - 1 Nov 1998

Pfister M H, Apaydin F, Turan O, Bereketoglu M, Bylgen V, Braendle U, Zenner H P, Lalwani A K

Abstract excerpt

X-linked inherited hearing impairment is a group of heterogeneous disorders accounting for less than 2% of hereditary hearing loss. DFN4, a sex-linked hearing impairment associated with profound sensorineural hearing loss, has been previously mapped to Xp21.2, a region containing the DMD locus. We have identified a family from Turkey with deafness in which the disease maps to and refines the DFN4 locus. In...

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Identifiers

PMID: 9799605
DOI: 10.1006/geno.1998.5538

Genes

DMD

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

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