Genetic analysis of a kindred with familial hypobetalipoproteinemia. Evidence for two separate gene defects: one associated with an abnormal apolipoprotein B species, apolipoprotein B-37; and a second associated with low plasma concentrations of apolipoprotein B-100.

Ítems similars

• Characterization of an abnormal species of apolipoprotein B, apolipoprotein B-37, associated with familial hypobetalipoproteinemia.
  per: Young, S G, et al.
  Publicat: (1987)
• A truncated species of apolipoprotein B (B67) in a kindred with familial hypobetalipoproteinemia.
  per: Welty, F K, et al.
  Publicat: (1991)
• Inference of a molecular defect of apolipoprotein B in hypobetalipoproteinemia by linkage analysis in a large kindred.
  per: Leppert, M, et al.
  Publicat: (1988)
• Targeted modification of the apolipoprotein B gene results in hypobetalipoproteinemia and developmental abnormalities in mice.
  per: Homanics, G E, et al.
  Publicat: (1993)
• Monoclonal antibody MB19 detects genetic polymorphism in human apolipoprotein B.
  per: Young, S G, et al.
  Publicat: (1986)