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Self-reported ethnicity/race based of 91 patients with autosomal dominant hypercholesterolemia (ADH). Maternal and paternal ancestor’s origins were used if provided by the patient. FH (familial hypercholesterolemia) denotes patients found to have LDLR mutations. FDB (familial defective apolipoprotein B) denotes patients found to have APOB mutations. Unexplained ADH denotes patients with ADH but no mutations in the known loci. ‘n’ indicates number of subjects.
