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Article

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

European journal of human genetics : EJHG - 1 Mar 2002

Mustapha Mirna, Chouery Eliane, Chardenoux Sébastien, Naboulsi Mohamed, Paronnaud Joël, Lemainque Arnaud, Mégarbané André, Loiselet Jacques, Weil Dominique, Lathrop Mark, Petit Christine

Abstract excerpt

We report the identification of a novel locus responsible for an autosomal recessive form of hearing loss (DFNB) segregating in a Palestinian consanguineous family from Jordan. The affected individuals suffer from profound prelingual sensorineural hearing impairment. A genetic linkage with polymorphic markers surrounding D9S1776 was detected, thereby identifying a novel deafness locus, DFNB31. This locus could be...

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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PMID: 11973626
DOI: 10.1038/sj.ejhg.5200780

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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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Research trail→

Click a neighbor to travelStep 1 · 12 closest

DFNB31, a recessive form of sensorineural hearing loss, maps to chromosome 9q32-34.PMID 11973626Read ↗

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

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

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

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

Deafness DFNB110 associated with a human MAP3K1 recessive variant recapitulates hearing loss of Map3k1 kinase deficient miceSemantic proximity Read ↗

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

Mutations in PTPRQ are a cause of autosomal-recessive nonsyndromic hearing impairment DFNB84 and associated with vestibular dysfunction.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 ↗

Refined localization of autosomal recessive nonsyndromic deafness DFNB10 locus using 34 novel microsatellite markers, genomic structure, and exclusion of six known genes in the region.Semantic proximity Read ↗

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

Identification of a novel compound heterozygous mutation in PTPRQ in a DFNB84 family with prelingual sensorineural hearing impairment.Semantic proximity Read ↗

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