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. 2010 Jun;51(6):1535–1545. doi: 10.1194/jlr.M002717

Fig. 5.

Fig. 5.

Identification of mutations in GPIHBP1. Filled symbols indicate family members with chylomicronemia. Black circles within the symbols indicate heterozygous carriers of GPIHBP1 mutations. Question mark indicates the lack of DNA sequencing in the son (II-1). Electropherograms including the two mutations, C65S and C68G, in exon 3 of GPIHBP1 are shown below the symbols to the right. Arrows indicate heterozygous changes.