Heterozygous lipoprotein lipase deficiency due to a missense mutation as the cause of impaired triglyceride tolerance with multiple lipoprotein abnormalities.

Podobne zapisy

• Linkage of low-density lipoprotein size to the lipoprotein lipase gene in heterozygous lipoprotein lipase deficiency.
  od: Hokanson, J E, i wsp.
  Wydane: (1999)
• Regulation of lipoprotein lipase-mediated lipolysis of triglycerides
  od: Basu, Debapriya, i wsp.
  Wydane: (2020)
• Phenotypic expression of heterozygous lipoprotein lipase deficiency in the extended pedigree of a proband homozygous for a missense mutation.
  od: Wilson, D E, i wsp.
  Wydane: (1990)
• Severe hypertriglyceridemia in a patient heterozygous for a lipoprotein lipase gene allele with two novel missense variants
  od: Kassner, Ursula, i wsp.
  Wydane: (2015)
• Familial chylomicronemia (type I hyperlipoproteinemia) due to a single missense mutation in the lipoprotein lipase gene.
  od: Ameis, D, i wsp.
  Wydane: (1991)