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Article

DFNB68, a novel autosomal recessive non-syndromic hearing impairment locus at chromosomal region 19p13.2.

Human genetics - 1 Aug 2006

Santos Regie Lyn P, Hassan Muhammad Jawad, Sikandar Shaheen, Lee Kwanghyuk, Ali Ghazanfar, Martin Protacio E, Wambangco Michael Angelo L, Ahmad Wasim, Leal Suzanne M

Abstract excerpt

From a large collection of families with autosomal recessive non-syndromic hearing impairment (NSHI) from Pakistan, linkage has been established for two unrelated consanguineous families to 19p13.2. This new locus was assigned the name DFNB68. A 10 cM genome scan and additional fine mapping were carried out using microsatellite marker loci. Linkage was established for both families to DFNB68 with maximum...

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Identifiers

PMID: 16703383
DOI: 10.1007/s00439-006-0188-z
PMCID: PMC2909094

Genes

KEAP1

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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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DFNB68, a novel autosomal recessive non-syndromic hearing impairment locus at chromosomal region 19p13.2.PMID 16703383Read ↗

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