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

*Corresponding author for this work

Research output: Contribution to journalJournal articleResearchpeer-review

Fingerprint Dive into the research topics of 'Evaluation of a clinically applicable mutation screening technique for genetic diagnosis of familial hypercholesterolemia and familial defective apolipoprotein B'. Together they form a unique fingerprint.

Medicine & Life Sciences