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. 2019 Aug 8;2019:2905739. doi: 10.1155/2019/2905739

Table 2.

PD genetic studies in Central Asian countries.

n Genetic mutations studied Analysis method Results Sample size Country (reference)
1 SNCA gene (Ala30Pro, Ala53Thr, Gly46Lis, Gly51Asp) PCR, gel electrophoresis No pathogenic mutations found 34 PD cases Kazakhstan [6]
2 GIGYF2 PCR, Sanger sequencing No pathogenic mutations found Not stated Kazakhstan [14]
3 SNCA (Ala53Thr), Parkin (T240M), LRRK2 (G2019S), Nat2, GSTT1, and GSTM1 PCR, Sanger sequencing G2019S was found in 5.7% of idiopathic PD and 17.6% of familial PD patients 153 PD cases, 80 controls Uzbekistan [15]
4 SNCA, Parkin Not stated 13 (19.4%) positive to SNCA gene mutation, 27 (40.3%) positive to Parkin mutation 67 Uzbekistan [16]

PCR, polymerase chain reaction; PD, Parkinson's disease.