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Hum Genet ; 120(1): 85-92, 2006 Aug.
Article in English | MEDLINE | ID: mdl-16703383

ABSTRACT

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 multipoint LOD scores of 4.8 and 4.6. The overlap of the homozygous regions between the two families was bounded by D19S586 and D19S584, which limits the locus interval to 1.9 cM and contains 1.4 Mb. The genes CTL2, KEAP1 and CDKN2D were screened but were negative for functional sequence variants.


Subject(s)
Chromosomes, Human, Pair 19/genetics , Genes, Recessive , Genetic Predisposition to Disease/genetics , Hearing Loss/genetics , Chromosome Mapping , Consanguinity , Family Health , Female , Genetic Linkage , Genotype , Humans , Intracellular Signaling Peptides and Proteins/genetics , Kelch-Like ECH-Associated Protein 1 , Lod Score , Male , Membrane Glycoproteins/genetics , Membrane Transport Proteins/genetics , Microsatellite Repeats , Pedigree , Sequence Analysis, DNA
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