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Published in 2022 at "Endokrynologia Polska"
DOI: 10.5603/ep.a2021.0109
Abstract: INTRODUCTION Familial hypercholesterolaemia (FH) is the most common autosomal genetic disease of cholesterol metabolism disorder. Proprotein convertase subtilisin/kexin type 9 (PCSK9) monoclonal antibody (mAb) is a new target lipid-regulating drug related to cholesterol metabolism that…
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Keywords:
familial hypercholesterolaemia;
hypercholesterolaemia;
effect pcsk9;
patients familial ... See more keywords