Some children with a familial hypercholesterolemia mutation may exhibit persistent low LDL levels

J Clin Lipidol. 2018 Sep-Oct;12(5):1327-1328. doi: 10.1016/j.jacl.2018.06.012. Epub 2018 Jun 28.
No abstract available

Publication types

  • Letter
  • Comment

MeSH terms

  • Child
  • Cohort Studies
  • Goals
  • Humans
  • Hyperlipoproteinemia Type II*
  • Mutation
  • Norway
  • Receptors, LDL / genetics

Substances

  • Receptors, LDL