Case-control study of patients with essential tremor in Latvia
Autor: | E. Vitols, Eriks Jankevics, Ilze Radovica, Ligita Smeltere, Inna Inashkina |
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Rok vydání: | 2008 |
Předmět: | |
Zdroj: | European Journal of Neurology. 15:988-990 |
ISSN: | 1468-1331 1351-5101 |
DOI: | 10.1111/j.1468-1331.2008.02225.x |
Popis: | Background: Essential tremor (ET) is the most prevalent inherited movement disorder. ET has been mapped on chromosomes 2 and 3, but causative genes are not known. Methods: We genotyped 16 microsatellite markers in a case–control cohort consisting of 104 patients and 116 controls. Results: No significant difference between allele frequencies was found. The highest difference of frequencies was found in allele 171 of the marker D2S220 (OR 0.13, 95% CI 0.02–1.03, P = 0.05). In addition, we investigated the distribution of suspected disease gene DRD3 Ser9Gly polymorphism in the same patients and controls. Conclusion: There was not a significant difference in genotypic distribution between disease group and control subjects (χ2 = 2.8, P = 0.25). |
Databáze: | OpenAIRE |
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