Evaluation of a clinically applicable mutation screening technique for genetic diagnosis of familial hypercholesterolemia and familial defective apolipoprotein B

Henrik Nissen*, Annebirthe B. Hansen, Per Guldberg, Torben S. Hansen, Niels E. Petersen, Mogens Hørder

*Kontaktforfatter for dette arbejde

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Medicin og biovidenskab