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- W2472202155 abstract "OBJECTIVES: Essential tremor (ET) is one of the most common neurological movement disorders. In more than half of the cases, ET is inherited in an auto-somal dominant manner, but no causative ET gene has been identified. However, several candidate loci have been reported, including the ETM2 locus that was originally found in a large American family of Czech descent. METHODS: To ascertain the association with ETM2, we performed a genetic analysis of three polymorphic loci, etm1231, etm1234, and etm1240, located within the ETM2 candidate region in 61 Czech patients with a family history of ET and 68 healthy controls. RESULTS: The allele frequencies were not significantly different between the patients and the controls, and we did not observe any haplotype specifically associated with ET. CONCLUSIONS: This is the first report on the genetics of familial essential tremor in Czech patients. Our findings provide further evidence of genetic heterogeneity for ET." @default.
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- W2472202155 date "2010-01-01" @default.
- W2472202155 modified "2023-10-16" @default.
- W2472202155 title "No association with the ETM2 locus in Czech patients with familial essential tremor." @default.
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