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The c.-237-236GA>TT THAP1 sequence variant does not increase risk for primary dystonia

  • Jianfeng Xiao
  • , Yu Zhao
  • , Robert W. Bastian
  • , Joel S. Perlmutter
  • , Brad A. Racette
  • , Samer D. Tabbal
  • , Morvarid Karimi
  • , Randal C. Paniello
  • , Zbigniew K. Wszolek
  • , Ryan J. Uitti
  • , Jay A. Van Gerpen
  • , David K. Simon
  • , Daniel Tarsy
  • , Peter Hedera
  • , Daniel D. Truong
  • , Karen P. Frei
  • , Andrew Blitzer
  • , Monika Rudzińska
  • , Ronald F. Pfeiffer
  • , Carrie Le
  • Mark S. Ledoux

Research output: Contribution to journalArticlepeer-review

Original languageEnglish
Pages (from-to)549-553
Number of pages5
JournalMovement Disorders
Volume26
Issue number3
DOIs
StatePublished - Feb 15 2011
Externally publishedYes

ASJC Scopus Subject Areas

  • Neurology
  • Clinical Neurology

Keywords

  • DYT6
  • Dystonia
  • High-resolution melting
  • THAP1
  • Untranslated region
  • Humans
  • Middle Aged
  • Male
  • Young Adult
  • Base Sequence
  • Aged, 80 and over
  • Adult
  • Female
  • Nuclear Proteins/genetics
  • Untranslated Regions/genetics
  • Child
  • Dystonic Disorders/etiology
  • Mutation/genetics
  • Gene Frequency
  • Genotype
  • DNA-Binding Proteins/genetics
  • Adolescent
  • Apoptosis Regulatory Proteins/genetics
  • Aged
  • White People/genetics

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