Fig. 1From: Genetic basis of index patients with familial hypercholesterolemia in Chinese population: mutation spectrum and genotype-phenotype correlationDistribution of different types of all the FH-related variances (n = 119) detected in the study. FH: familial hypercholesterolemia; LDLR: low-density lipoprotein receptor; APOB: apolipoprotein B; PCSK9: proprotein convertase subtilisin/Kexin type 9Back to article page