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an increasing number of disease genes/pathogenic mutations are being identified in PD patients by means of whole genome sequencing (WGS) or whole exome sequencing (WES) studies 8 , and both autosomal recessive and dominant forms have been described among the monogenic forms of PD

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would like to acknowledge Deutsche Forschungsgemeinschaft (DFG, German Research Foundation) for financial support (SFB/TRR 298 SIIRI Project-ID 426335750)

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