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. Author manuscript; available in PMC: 2021 Nov 22.
Published in final edited form as: Parkinsonism Relat Disord. 2021 Jun 29;89:63–72. doi: 10.1016/j.parkreldis.2021.06.023

Fig. 2.

Fig. 2.

Haplotype analysis. Genotyping across the SNCA locus reveals a haplotype shared among the tested SNCA carriers, indicated in dark green. Allele counts and frequencies in the 56 Turkish individuals are also shown. Genomic positions are annotated according to the Genome Reference Consortium human genome build 38 (GRCh38). NA: not available; -: absent.