Figure 1From: Peroxisomal proliferator activated receptor-γ deficiency in a Canadian kindred with familial partial lipodystrophy type 3 (FPLD3) A Canadian multigenerational FPLD3 kindred. Darkened symbols indicate affected individuals, each of whom was later confirmed to be heterozygous for the respective PPARG nonsense mutation. Dots inside white symbols indicate normal PPARG genotype. Subject identification number and age in years are shown below the appropriate symbols.Back to article page