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), multiple system atrophy (MSA), spastic paraplegias (HSP) and repeat expansion disorders (RED) with a range of wet lab techniques from DNA and RNA extraction to fragment analysis, and exome sequencing and
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perturbation, to unravel disease relevant pathways. We will perform a genome-wide association (GWA) analysis complemented by long read sequencing to identify genetic modifiers of onset, phenotype and progression
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