Literature DB >> 12210890

Familial essential tremor is not associated with SCA-12 mutation in southern Italy.

Giuseppe Nicoletti1, Grazia Annesi, Sara Carrideo, Carmine Tomaino, Alfonso Di Costanzo, Mario Zappia, Aldo Quattrone.   

Abstract

We investigated 30 patients with familial essential tremor (ET) for spinocerebellar ataxia type 12 (SCA-12) mutations. No patient presented a CAG repeat larger than 19, suggesting that familial ET and SCA-12 are distinct diseases. Copyright 2002 Movement Disorder Society

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Year:  2002        PMID： 12210890     DOI： 10.1002/mds.10191

Source DB:  PubMed          Journal:  Mov Disord        ISSN： 0885-3185            Impact factor:   10.338


  3 in total

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

Authors:  L N Clark; X Ye; X Liu; K Mirzozoda; E D Louis
Journal:  Parkinsonism Relat Disord       Date:  2015-06-06       Impact factor: 4.891

2.  Clinical Characterization of Genetically Diagnosed Cases of Spinocerebellar Ataxia Type 12 from India.

Authors:  Supriyo Choudhury; Sayan Chatterjee; Koustav Chatterjee; Rebecca Banerjee; Jonathan Humby; Banashree Mondal; Sidharth S Anand; Shantanu Shubham; Hrishikesh Kumar
Journal:  Mov Disord Clin Pract       Date:  2017-11-01

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
Journal:  Pharmaceuticals (Basel)       Date:  2021-05-27
  3 in total

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