Clinical Genetics · 2004 · 25 citations · 27 references
Life SciencesGeneticsMolecular GeneticsHuman GeneticsMedical GeneticsNeurogeneticsDisease Susceptibility LociGenetic DisordersHaplotype AnalysisNeurogenetic DisordersEssential TremorEssential Tremor GeneticsFamilial TremorGenetic Basis Of TremorHaplotype Frequency AnalysisHaplotype Mapping
An ancestral haplotype on chromosome 2p24.1 described in an American sample with familial essential tremor (ET) was analyzed in a different ethnic sample from Singapore. Six polymorphic loci (etm1240, etm1231, etm1234, APOB, etm1241, and etm1242) in a 274-kb interval within an ET gene candidate region (ETM2) were analyzed in Singaporean individuals with a family history of ET (n = 52) and compared to Singaporean controls older than age 65 (n = 49). The allele frequencies were significantly different between cases and controls for the loci etm1234 (p = 0.0001) and APOB (p = 0.0320). An extended haplotype formed by the loci etm1231, etm1234, and APOB occurred with a frequency of 31% in Singaporean cases and in 1.8% of elderly Singaporean controls (p = 0.0005). Haplotype studies in two different population samples suggest that a disease locus for ET lies near or within the 100-kb interval between the loci etm1231 and APOB.
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Mapping of a familial essential tremor gene, FET1, to chromosome 3q13
Gulcher, Augustine Kong, Kristleifur Kristjánsson et al. · Nature Genetics · 1997 · 290 citations
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Medicine, Neurobiology, Neurology +12
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Okan Doğu, Serhan Sevim, Handan Çamdeviren et al. · Neurology · 2003 · 232 citations