Association between a specific apolipoprotein B mutation and familial defective apolipoprotein B-100.

Ítems similars

• Haplotype analysis of the human apolipoprotein B mutation associated with familial defective apolipoprotein B100.
  per: Ludwig, E H, et al.
  Publicat: (1990)
• Familial defective apolipoprotein B-100: low density lipoproteins with abnormal receptor binding.
  per: Innerarity, T L, et al.
  Publicat: (1987)
• Familial defective apolipoprotein B-100: enhanced binding of monoclonal antibody MB47 to abnormal low density lipoproteins.
  per: Weisgraber, K H, et al.
  Publicat: (1988)
• Decreased Bone Mineral Density in Subjects Carrying Familial Defective Apolipoprotein B-100
  per: Yerges-Armstrong, Laura M., et al.
  Publicat: (2013)
• High-resolution analysis of a hypervariable region in the human apolipoprotein B gene.
  per: Ludwig, E H, et al.
  Publicat: (1989)