A newly identified null allelic mutation in the human lipoprotein lipase (LPL) gene of a compound heterozygote with familial LPL deficiency

Biochim Biophys Acta. 1992 Apr 14;1138(4):353-6. doi: 10.1016/0925-4439(92)90015-f.

Abstract

In a Japanese patient with familial LPL deficiency, a new null allelic mutation, one base pair deletion at nucleotide position 916 was identified in exon 5 of one allele. In exon 3 of the other allele, we found the same nonsense mutation as we described previously in other Japanese kindreds. For the deletional mutant allele, we developed a simple detection method and constructed the DNA haplotype.

MeSH terms

  • Alleles
  • Amino Acid Sequence
  • Asian People / genetics
  • Base Sequence
  • Female
  • Heterozygote
  • Humans
  • Hyperlipoproteinemia Type I / enzymology*
  • Hyperlipoproteinemia Type I / genetics
  • Lipoprotein Lipase / deficiency
  • Lipoprotein Lipase / genetics*
  • Lipoprotein Lipase / metabolism
  • Male
  • Molecular Sequence Data
  • Mutation / genetics
  • Polymerase Chain Reaction

Substances

  • Lipoprotein Lipase