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ATXN10 Microsatellite Distribution in a Peruvian Amerindian Population

  • Diego Véliz-Otani(corresponding author)
    ,
  • Miguel Inca-Martinez
    ,
  • Giovana B. Bampi
    ,
  • Olimpio Ortega
    ,
  • Laura B. Jardim
    ,
  • Maria Luiza Saraiva-Pereira
*Corresponding author for this work
  • docencia y atención especializada en epilepsia
    ,
  • Cleveland Clinic Foundation
    ,
  • Federal University of Rio Grande do Sul
    ,
  • Universidade Federal Do Rio Grande Do sul
    ,
  • Universidad Peruana Cayetano Heredia
Research Output:
Contribution to journal
Article
Peer-review

Publication Information

Output type

Research Output:
Contribution to journal
Article
Peer-review

Original language

English

Pages from-to (Number of pages)

Pages 841-848 (8 pages)

Journal (Volume, Issue Number)

Cerebellum (Volume 18, Issue 5)

Publication milestones

  • Published - 01/10/2019

Publication status

Published - 01/10/2019

ISSN

1473-4222

Publication IDs

  • Scopus: 85069640701
  • PubMed: 31342269

Abstract

Spinocerebellar ataxia type 10 (SCA10) is a repeat expansion disease occurring mostly in Latin America, suggesting that the mutation spread with the peopling of the Americas, or that Amerindian populations, have a higher ATXN10 mutability. High frequency of large normal alleles is associated with prevalence and relative frequency of other repeat expansion diseases. To test whether the allele distribution of the SCA10-causing ATXN10 microsatellite in an Amerindian Peruvian population differs from that of other populations. The ATXN10 allele distribution in a Quechua Peruvian population from Puno, Peru, is similar to that of Finland. Mean allele size and mode were also similar to those of Mexico, Japan, and white Europeans. ATXN10 allele distribution in a healthy Amerindian population from Peru does not differ from that of other populations.