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. 2014 Apr 10;9(4):e94697. doi: 10.1371/journal.pone.0094697

Figure 1. Pedigree and mutations of a hypercholesterolemic family.

Figure 1

Arrow denotes the proband. Shaded and partially shaded shapes denote compound heterozygotes and heterozygotes with different mutations, respectively. The exon 8 c.1129 G>T and exon 9 c.1268 T>C mutations are depicted on the right.