A missense mutation at codon 188 of the human lipoprotein lipase gene is a frequent cause of lipoprotein lipase deficiency in persons of different ancestries.

مواد مشابهة

• Partial gene duplication involving exon-Alu interchange results in lipoprotein lipase deficiency.
  بواسطة: Devlin, R H, وآخرون
  منشور في: (1990)
• The lipoprotein lipase Gly188----Glu mutation in South Africans of Indian descent: evidence suggesting common origins and an increased frequency.
  بواسطة: Henderson, H E, وآخرون
  منشور في: (1992)
• A major insertion accounts for a significant proportion of mutations underlying human lipoprotein lipase deficiency.
  بواسطة: Langlois, S, وآخرون
  منشور في: (1989)
• Heterozygous lipoprotein lipase deficiency due to a missense mutation as the cause of impaired triglyceride tolerance with multiple lipoprotein abnormalities.
  بواسطة: Miesenböck, G, وآخرون
  منشور في: (1993)
• Coexistence of abnormalities of hepatic lipase and lipoprotein lipase in a large family.
  بواسطة: Auwerx, J H, وآخرون
  منشور في: (1990)