No association with the ETM2 locus in Czech patients with familial essential tremor.

Zahorakova D, Ulmanova O, Kemlink D, Kofrankova M, Roth J, Martasek P, Ruzicka E.

Journal Article 2010; 31(4): 549-552 PubMed PMID: 20802447 Keywords: Aged, Aged, 80 and over, Alleles, Czech Republic, Essential Tremor:genetics, Female, Gene Frequency, Genetic Association Studies, Genetic Heterogeneity, Genetic Loci, Genetic Predisposition to Disease, Genotype, Haplotypes, Humans, Male, Microsatellite Re.

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 autosomal 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 Amer.....

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Vol. 31 (4) 2010 Neuro endocrinology letters

No association with the ETM2 locus in Czech patients with familial essential tremor.

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