Homozygous familial hypercholesterolemia due to APOB genetic variant with unusual clinical course

Kardiol Pol. 2021;79(9):1030-1031. doi: 10.33963/KP.a2021.0034. Epub 2021 Jun 14.
No abstract available

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Apolipoprotein B-100
  • Apolipoproteins B / genetics
  • Homozygote
  • Humans
  • Hyperlipoproteinemia Type II* / diagnosis
  • Hyperlipoproteinemia Type II* / genetics
  • Mutation

Substances

  • APOB protein, human
  • Apolipoprotein B-100
  • Apolipoproteins B