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Article

Genomic structures of SCN2A and SCN3A - candidate genes for deafness at the DFNA16 locus.

Gene - 7 Feb 2001

Kasai N, Fukushima K, Ueki Y, Prasad S, Nosakowski J, Sugata K, Sugata A, Nishizaki K, Meyer N C, Smith R J

Abstract excerpt

DFNA16 is a form of autosomal dominant non-syndromic hearing loss (ADNSHL) characterized by fluctuating progressive hearing impairment. Earlier, we mapped the deafness-causing gene to chromosome 2q23-24.3. In this paper, we describe fine mapping results using additional markers tightly linked to...

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PMID: 11245985
DOI: 10.1016/s0378-1119(00)00594-1

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STS

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026. Prepared record publication-11245985-2026-09-01.1. Manifest publication-graph-cohort-2026-09-01.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 1 Sept 2026.

Related research

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Research trail→

Click a neighbor to travelStep 1 · 12 closest

Genomic structures of SCN2A and SCN3A - candidate genes for deafness at the DFNA16 locus.PMID 11245985Read ↗

A gene for fluctuating, progressive autosomal dominant nonsyndromic hearing loss, DFNA16, maps to chromosome 2q23-24.3.Semantic proximity Read ↗

Mapping of a new autosomal dominant nonsyndromic hearing loss locus (DFNA30) to chromosome 15q25-26.Semantic proximity Read ↗

DFNB89, a novel autosomal recessive nonsyndromic hearing impairment locus on chromosome 16q21-q23.2.Semantic proximity Read ↗

Further evidence for a third deafness gene within the DFNA2 locus.Semantic proximity Read ↗

Refining the DFNB17 interval in consanguineous Indian families.Semantic proximity Read ↗

Screening of the DFNB3 locus: identification of three novel mutations of MYO15A associated with hearing loss and further suggestion for two distinctive genes on this locus.Semantic proximity Read ↗

Association of unconventional myosin MYO15 mutations with human nonsyndromic deafness DFNB3.Semantic proximity Read ↗

Genetic mapping refines DFNB3 to 17p11.2, suggests multiple alleles of DFNB3, and supports homology to the mouse model shaker-2.Semantic proximity Read ↗

Phenotypic consequences of gene disruption by a balanced de novo translocation involving SLC6A1 and NAA15.Semantic proximity Read ↗

A gene for congenital, recessive deafness DFNB3 maps to the pericentromeric region of chromosome 17.Semantic proximity Read ↗

An autosomal recessive nonsyndromic form of sensorineural hearing loss maps to 3p-DFNB6.Semantic proximity Read ↗

Fine mapping of autosomal dominant nonsyndromic hearing impairment DFNA21 to chromosome 6p24.1-22.3.Semantic proximity Read ↗

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