A sensorineural progressive autosomal recessive form of isolated deafness, DFNB13, maps to chromosome 7q34-q36.

doi:10.1038/sj.ejhg.5200177

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Article

A sensorineural progressive autosomal recessive form of isolated deafness, DFNB13, maps to chromosome 7q34-q36.

European journal of human genetics : EJHG - 1 Jan 2000

Mustapha M, Chardenoux S, Nieder A, Salem N, Weissenbach J, el-Zir E, Loiselet J, Petit C

Abstract excerpt

Deafness is the most frequent sensorineural defect in children. The vast majority of the prelingual forms of isolated deafness are highly genetically heterogeneous with an autosomal recessive mode of inheritance. Using linkage analysis, we have mapped the gene responsible for a severe progressive...

Topics

Chromosome Mapping
Chromosomes, Human, Pair 7
Deafness
Female
Genes, Recessive
Genetic Linkage
Genotype
Hereditary Sensory and Autonomic Neuropathies
Homozygote
Humans
Male
Pedigree

Source

Open in PubMed

Identifiers

PMID: 9781028
DOI: 10.1038/sj.ejhg.5200177

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 30 Aug 2026. Prepared record publication-9781028-2026-08-30.1. Manifest publication-graph-cohort-2026-08-30.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 30 Aug 2026.

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