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Article

Localization of a novel autosomal recessive non-syndromic hearing impairment locus DFNB55 to chromosome 4q12-q13.2.

Clinical genetics - 1 Sept 2005

Irshad S, Santos R L P, Muhammad D, Lee K, McArthur N, Haque S, Ahmad W, Leal S M

Abstract excerpt

Hereditary hearing impairment (HI) is the most genetically heterogeneous trait known in humans. So far, 54 autosomal recessive non-syndromic hearing impairment (ARNSHI) loci have been mapped, and 21 ARNSHI genes have been identified. Here is reported the mapping of a novel ARNSHI locus, DFNB55, t...

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Identifiers

PMID: 16098016
DOI: 10.1111/j.1399-0004.2005.00492.x
PMCID: PMC2910366

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-16098016-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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