Figure 3From: Peroxisomal proliferator activated receptor-γ deficiency in a Canadian kindred with familial partial lipodystrophy type 3 (FPLD3) Genomic DNA sequence electropherograms of heterozygous PPARG mutation. The bottom electropherogram tracing shows both alleles in subject II-5 from kindred 1 (Y355X), compared to sequence from a healthy subject. The position of the mutation is indicated by the arrow. Normal nucleotide and amino acid sequence is shown above the wild type electropherogram tracing.Back to article page