Fig. 2From: Genetic basis of index patients with familial hypercholesterolemia in Chinese population: mutation spectrum and genotype-phenotype correlationComparison of FH-related mutations according to DLCN score. FH: familial hypercholesterolemia; DLCN: Dutch Lipid Clinic Network; LDLR: low-density lipoprotein receptor; APOB: apolipoprotein B; PCSK9: proprotein convertase subtilisin/Kexin type 9Back to article page