Catalina Dussaillant

Summary

Publications

  1. pmc APOA5 Q97X mutation identified through homozygosity mapping causes severe hypertriglyceridemia in a Chilean consanguineous family
    Catalina Dussaillant
    Department of Nutrition, Diabetes and Metabolism, School of Medicine, Pontificia Universidad Catolica de Chile, Alameda, Santiago, Chile
    BMC Med Genet 13:106. 2012

Detail Information

Publications1

  1. pmc APOA5 Q97X mutation identified through homozygosity mapping causes severe hypertriglyceridemia in a Chilean consanguineous family
    Catalina Dussaillant
    Department of Nutrition, Diabetes and Metabolism, School of Medicine, Pontificia Universidad Catolica de Chile, Alameda, Santiago, Chile
    BMC Med Genet 13:106. 2012
    ..The aim of this study was to determine the genetic locus responsible for the severe HTG in this family...