Genetic heterogeneity in familial hypercholesterolemia: evidence for two different mutations affecting functions of low-density lipoprotein receptor.

Ítems similars

• Esterification of Low Density Lipoprotein Cholesterol in Human Fibroblasts and Its Absence in Homozygous Familial Hypercholesterolemia
  per: Goldstein, Joseph L., et al.
  Publicat: (1974)
• Genetics of the low density lipoprotein receptor. Diminished receptor activity in lymphocytes from heterozygotes with familial hypercholesterolemia.
  per: Bilheimer, D W, et al.
  Publicat: (1978)
• Evidence for a dominant gene that suppresses hypercholesterolemia in a family with defective low density lipoprotein receptors.
  per: Hobbs, H H, et al.
  Publicat: (1989)
• Reduction in cholesterol and low density lipoprotein synthesis after portacaval shunt surgery in a patient with homozygous familial hypercholesterolemia.
  per: Bilheimer, D W, et al.
  Publicat: (1975)
• Degradation of cationized low density lipoprotein and regulation of cholesterol metabolism in homozygous familial hypercholesterolemia fibroblasts.
  per: Basu, S K, et al.
  Publicat: (1976)