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Published in 2022 at "Frontiers in Genetics"
DOI: 10.3389/fgene.2022.849008
Abstract: Introduction: The cause of familial hypercholesterolemia (FH) is defect in LDL receptor or familial defect of apolipoprotein B-100 (FDB) or, rarely, defect in proprotein convertase subtilisin/kexin type 9. Identification and treatment of patients with FH…
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Keywords:
fdb;
lipid clinic;
retrospective analysis;
mmol ... See more keywords