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. 2010 Sep 13;107(39):16970–16975. doi: 10.1073/pnas.1011751107

Fig. 5.

Fig. 5.

Genetic studies in human patients identify a PD-associated variance in SAT1. (A) Schematic of the SAT1 gene and the location of the deletion within the 3′UTR of SAT1. (B) Sequence chromatograms showing a PD patient heterozygous for the c.786_788delTGT variant, and (C) a wild-type subject.