Phenotypic expression and frequency of familial defective apolipoprotein B-100 in Belgian hypercholesterolemics

Author:

Kotze M.J.,Peeters A.V.,Langenhoven E.,Wauters J.G.,Van Gaal L.F.

Publisher

Elsevier BV

Subject

Cardiology and Cardiovascular Medicine

Reference41 articles.

1. Familial defective apolipoprotein B-100: low density lipoproteins with abnormal receptor binding;Innerarity,1987

2. Association between a specific apolipoprotein B mutation and familial defective apolipoprotein B-100;Soria,1989

3. Demonstration that the Arg2500 — Gln mutation is the cause of familial defective apolipoprotein B 100, using a cell culture expression system for the synthesis of recombinant human LDL;Innerarity;Circulation,1993

4. Familial ligand-defective apolipoprotein B: Identification of a new mutation that decreases LDL receptor binding affinity;Pullinger;Circulation,1993

5. Familial defective apolipoprotein B-100. Comparison with familial hypercholesterolemia in 18 cases detected in Munich;Schuster;Arteriosclerosis,1990

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