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Although the primary causes of FH are mutations in the LDLR gene (representing 60%80% of FH patients), mutations in the apolipoprotein B (APOB) gene that cause familial ligand-defective apoB (often referred to as familial hypercholesterolemia type 2) and gain-of-function mutations in the proprotein convertase subtilisin/kexin type 9 (PCSK9) gene are also associated with autosomal dominant forms of familial hypercholesterolemia
Make sure to wipe the working area and bottle tops with rubbing alcohol
Take this medication for the entire amount of time recommended by your doctor to see signs that accutane is working
