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. 2015 Jul 27;10(4):1450–1454. doi: 10.3892/etm.2015.2659

Figure 1.

Figure 1.

Electrophoresis results of the G2019S mutation in exon 41 of the LRRK2 gene digested with ScfI. Electrophoresis results of the R1441C mutation in exon 31 of the LRRK2 gene digested with BstU1. M, DNA marker 500 bp in length; 1–7, dominant hereditary sporadic PD patients.