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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 sensorineural hearing loss, DFNB13, segregating in a large consanguineous family living in an isolated region in...

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Identifiers

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

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

Source receipt: pubmed, retrieved 7 Sept 2026.

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A sensorineural progressive autosomal recessive form of isolated deafness, DFNB13, maps to chromosome 7q34-q36.PMID 9781028Read ↗

Refined mapping of the autosomal recessive non-syndromic deafness locus DFNB13 using eight novel microsatellite markers.Semantic proximity Read ↗

DFNB31, a recessive form of sensorineural hearing loss, maps to chromosome 9q32-34.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 ↗

[A new locus for an autosomal dominant, non-syndromic hearing impairment (DFNA57) located on chromosome 19p13.2 and overlapping with DFNB15].Semantic proximity Read ↗

Linkage studies of non-syndromic recessive deafness (NSRD) in a family originating from the Mirpur region of Pakistan maps DFNB1 centromeric to D13S175.Semantic proximity Read ↗

A novel locus for autosomal recessive nonsyndromic hearing impairment, DFNB63, maps to chromosome 11q13.2-q13.4.Semantic proximity Read ↗

Two different connexin 26 mutations in an inbred kindred segregating non-syndromic recessive deafness: implications for genetic studies in isolated populations.Semantic proximity Read ↗

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

A novel autosomal recessive nonsyndromic hearing impairment locus (DFNB42) maps to chromosome 3q13.31-q22.3.Semantic proximity Read ↗

Mapping of a novel autosomal recessive nonsyndromic deafness locus (DFNB46) to chromosome 18p11.32-p11.31.Semantic proximity Read ↗

DFNB40, a recessive form of sensorineural hearing loss, maps to chromosome 22q11.21-12.1.Semantic proximity Read ↗

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