Heterogeneous mutations in the human lipoprotein lipase gene in patients with familial lipoprotein lipase deficiency.

Podobne zapisy

• Detection of familial LPL deficiency by PvuII RFLP.
  od: Gotoda, T, i wsp.
  Wydane: (1989)
• Familial lipoprotein lipase deficiency – neonatal presentation
  od: Siu-ying, Nip
  Wydane: (2015)
• Overexpression of apolipoprotein E in transgenic mice: marked reduction in plasma lipoproteins except high density lipoprotein and resistance against diet-induced hypercholesterolemia.
  od: Shimano, H, i wsp.
  Wydane: (1992)
• Suppression of diet-induced atherosclerosis in low density lipoprotein receptor knockout mice overexpressing lipoprotein lipase.
  od: Shimada, M, i wsp.
  Wydane: (1996)
• Lipoprotein lipase deficiency resulting from a nonsense mutation in exon 3 of the lipoprotein lipase gene.
  od: Emi, M, i wsp.
  Wydane: (1990)