Figure 2From: APOA5 Q97X Mutation Identified through homozygosity mapping causes severe hypertriglyceridemia in a Chilean consanguineous family Homozygous and heterozygous regions determined through homozygosity mapping in a consanguineous Chilean family with hypertriglyceridemia. Chr: chromosome; Numbers, 11: proband; 12: affected sister; 13 and 14: nonaffected siblings; 7: mother; Solid regions: heterozygosity in markers; Open regions: homozygosity in markers.Back to article page