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DFNB68, a novel autosomal recessive non-syndromic hearing impairment locus at chromosomal region 19p13.2.
- Source :
-
Human genetics [Hum Genet] 2006 Aug; Vol. 120 (1), pp. 85-92. Date of Electronic Publication: 2006 May 16. - Publication Year :
- 2006
-
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.
- Subjects :
- 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
Chromosomes, Human, Pair 19 genetics
Genes, Recessive
Genetic Predisposition to Disease genetics
Hearing Loss genetics
Subjects
Details
- Language :
- English
- ISSN :
- 0340-6717
- Volume :
- 120
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Human genetics
- Publication Type :
- Academic Journal
- Accession number :
- 16703383
- Full Text :
- https://doi.org/10.1007/s00439-006-0188-z