| Autor: |
Bel Hadj Ali I; Unité d'Epidémiologie Génétique et Moléculaire, Faculté de Médecine, 1007, Tunis, Tunisia., Thys M, Beltaief N, Schrauwen I, Hilgert N, Vanderstraeten K, Dieltjens N, Mnif E, Hachicha S, Besbes G, Ben Arab S, Van Camp G |
| Jazyk: |
angličtina |
| Zdroj: |
Human genetics [Hum Genet] 2008 Apr; Vol. 123 (3), pp. 267-72. Date of Electronic Publication: 2008 Jan 26. |
| DOI: |
10.1007/s00439-008-0470-3 |
| Abstrakt: |
Otosclerosis is a common disorder of the otic capsule resulting in hearing impairment in 0.3-0.4% of the Caucasian population. The aetiology of the disease remains unclear. In most cases, otosclerosis can be considered as a complex disease. In some cases, the disease is inherited as an autosomal dominant trait, sometimes with reduced penetrance. To date, seven autosomal dominant loci have been reported, but none of the disease-causing genes has been identified. In this study, we present the results of a genome-wide linkage analysis in a large Tunisian family segregating autosomal dominant otosclerosis. Linkage analysis localised the responsible gene to chromosome 9p13.1-9q21.11 with a maximal LOD score of 4.13, and this locus was named OTSC8. Using newly generated short tandem repeat polymorphism markers, we mapped this new otosclerosis locus to a 34.16 Mb interval between the markers D9S970 and D9S1799. This region comprises the pericentromeric region on both arms of chromosome 9, a highly complex region containing many duplicated sequences. |
| Databáze: |
MEDLINE |
| Externí odkaz: |
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