Variable expression of familial dysbetalipoproteinemia in apolipoprotein E*2 (Lys146-->Gln) Allele carriers.

Những quyển sách tương tự

• Familial dysbetalipoproteinemia associated with apolipoprotein E3-Leiden in an extended multigeneration pedigree.
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• Apolipoprotein e4 allele and cognitive decline in elderly men.
  Bằng: Feskens, E. J., et al.
  Được phát hành: (1994)
• Metabolism of apolipoproteins B-48 and B-100 of triglyceride-rich lipoproteins in patients with familial dysbetalipoproteinemia.
  Bằng: Stalenhoef, A F, et al.
  Được phát hành: (1986)
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• Identification of a new structural variant of human apolipoprotein E, E2(Lys146 leads to Gln), in a type III hyperlipoproteinemic subject with the E3/2 phenotype.
  Bằng: Rall, S C, et al.
  Được phát hành: (1983)