Literature DB >> 26077168

Genetic analysis of ten common degenerative hereditary ataxia loci in patients with essential tremor.

L N Clark1, X Ye2, X Liu3, K Mirzozoda4, E D Louis5.   

Abstract

BACKGROUND: To investigate the association of repeat expansion size in 10 common degenerative hereditary ataxia genes with essential tremor. These genes were spinocerebellar ataxia (SCA)-1 (ATXN1), SCA-2 (ATXN2), SCA-3 (ATXN3), SCA-6 (CACNA1A), SCA-7 (ATXN7), SCA-8 (ATXN8OS), SCA-10 (ATXN10), SCA-12 (PPP2R2B), SCA-17 (TBP) and dentatorubral-pallidolysian atrophy (DRPLA) (ATN1).
METHODS: Genetic analysis of repeat size in 10 degenerative hereditary ataxia loci was performed in 323 essential tremor patients and 299 controls enrolled at Columbia University. To test for differences in the allele distribution between patients and controls, a CLUMP analysis was performed.
RESULTS: None of the essential tremor patients had a repeat expansion in the intermediate or pathogenic range. Significant differences in the distribution of repeats in the 'normal' range for SCA2 and SCA8 (both p ≤ 0.02) were observed between essential tremor patients and controls.
CONCLUSIONS: Our study suggests that pathogenic repeat expansions in SCA loci are not associated with essential tremor.
Copyright © 2015 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  CAG repeat expansions; Essential tremor; Genetics; Spinocerebellar ataxia loci

Mesh:

Substances:

Year:  2015        PMID: 26077168      PMCID: PMC4572894          DOI: 10.1016/j.parkreldis.2015.06.004

Source DB:  PubMed          Journal:  Parkinsonism Relat Disord        ISSN: 1353-8020            Impact factor:   4.891


  12 in total

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Authors:  Elan D Louis; Joaquim J Ferreira
Journal:  Mov Disord       Date:  2010-04-15       Impact factor: 10.338

4.  Monte Carlo tests for associations between disease and alleles at highly polymorphic loci.

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6.  Essential tremor in twins: an assessment of genetic vs environmental determinants of etiology.

Authors:  C M Tanner; S M Goldman; K E Lyons; D A Aston; J W Tetrud; M D Welsh; J W Langston; W C Koller
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7.  Genetic analysis of SCA 2 and 3 repeat expansions in essential tremor and atypical Parkinsonism.

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Review 8.  Autosomal dominant cerebellar ataxias: clinical features, genetics, and pathogenesis.

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9.  Are interrupted SCA2 CAG repeat expansions responsible for parkinsonism?

Authors:  P Charles; A Camuzat; N Benammar; F Sellal; A Destée; A-M Bonnet; S Lesage; I Le Ber; G Stevanin; A Dürr; A Brice
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10.  Familial essential tremor is not associated with SCA-12 mutation in southern Italy.

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Journal:  Mov Disord       Date:  2002-07       Impact factor: 10.338

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  3 in total

Review 1.  Essential Tremor Within the Broader Context of Other Forms of Cerebellar Degeneration.

Authors:  Elan D Louis; Phyllis L Faust
Journal:  Cerebellum       Date:  2020-12       Impact factor: 3.847

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Review 3.  Genomic Markers for Essential Tremor.

Authors:  Félix Javier Jiménez-Jiménez; Hortensia Alonso-Navarro; Elena García-Martín; Ignacio Álvarez; Pau Pastor; José A G Agúndez
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