Autosomal dominant hypercholesterolemia (ADH) is a human disorder characterized phenotypically by isolated high-cholesterol levels. Mutations in the low density lipoprotein receptor (LDLR). APOB. and proprotein convertase subtilisin/kexin type 9 (PCSK9) genes are well known to be associated with the disease. https://pipingrockers.shop/product-category/niacin/