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Figure 1 | BMC Medical Genetics

Figure 1

From: APOA5 Q97X Mutation Identified through homozygosity mapping causes severe hypertriglyceridemia in a Chilean consanguineous family

Figure 1

Clinical characteristics and haplotypes of the APOA5 gene and its flanking region in a consanguineous Chilean family with hypertriglyceridemia. Arrow: proband (subject 11); Solid symbols: patients with triglycerides (TG) >56 mmol/L; Grey-filled symbols: patients with 5.6 < TG < 22 mmol/L; Double line: consanguineous marriage. Rs numbers represents SNPs flanking the APOA5 gene. In table: Grey-filled columns: patients with severe chylomicronemia (TG >56 mmol/L), homozygous for 97X mutation; * Tests taken on 2006; TG: Triglycerides; BMI: Body Mass Index; ND: Not Determined; Plasma Apo C-III normal range: 1.2 – 17.2 mg/dL. * Subject`s 8 haplotype was inferred from relative’s haplotypes.

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