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A gene (ETM) for essential tremor maps to chromosome2p22-p25
- Source :
- Movement Disorders. 12:859-864
- Publication Year :
- 1997
- Publisher :
- Wiley, 1997.
-
Abstract
- We report the results of linkage analysis in a large American family of Czech descent with dominantly inherited "Pure" essential tremor (ET) and genetic anticipation. Genetic loci on chromosome 2p22‐p25 establish linkage to this region with a maximum LOD score (Zmax) = 5.92 for the locus, D2S272. Obligate recombinant events place the ETM gene in a 15‐cM candidate interval between the genetic loci D2S168 and D2S224. Repeat expansion detection analysis suggests that expanded CAG trinucleotide sequences are associated with ET. These findings will facilitate the search for an ETM gene and may further our understanding of the human motor system.
- Subjects :
- Adult
X Chromosome
Adolescent
Genetic Linkage
Chromosome Disorders
Locus (genetics)
Biology
Severity of Illness Index
Trinucleotide Repeats
Genetic linkage
Tremor
medicine
Humans
Child
Gene
X chromosome
LINGO1
Aged
Czech Republic
Chromosome Aberrations
Genetics
Essential tremor
Haplotype
Middle Aged
medicine.disease
United States
Pedigree
Phenotype
Haplotypes
Neurology
Chromosomes, Human, Pair 2
Neurology (clinical)
Trinucleotide repeat expansion
Subjects
Details
- ISSN :
- 15318257 and 08853185
- Volume :
- 12
- Database :
- OpenAIRE
- Journal :
- Movement Disorders
- Accession number :
- edsair.doi.dedup.....8075d2e859ba11a80c7e91512f528bf8
- Full Text :
- https://doi.org/10.1002/mds.870120605