1.P.258 Mutation screening in patients with a phenotype of...

1.P.258 Mutation screening in patients with a phenotype of familial hypercholesterolemia and normal values in a functional LDL receptor/apolipoprotein B assay

H. Nissen, S. Lestavel, T.S. Hansen, G. Luc, E. Bruckert, V. Clavey
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Volume:
134
Year:
1997
Language:
english
DOI:
10.1016/s0021-9150(97)88439-0
File:
PDF, 195 KB
english, 1997
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