A novel mutation of apolipoprotein B in a French Canadian family with homozygous hypobetalipoproteinemia

J Clin Lipidol. 2011 Sep-Oct;5(5):414-7. doi: 10.1016/j.jacl.2011.06.014. Epub 2011 Jun 28.
No abstract available

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Apolipoproteins B / genetics*
  • Canada
  • Female
  • Genotype
  • Homozygote
  • Humans
  • Hypobetalipoproteinemias / genetics*
  • Mutation, Missense*
  • Sequence Analysis, DNA

Substances

  • Apolipoproteins B