Department Of Medical And Molecular Genetics 1

1. Author Correction: Elucidating causative gene variants in hereditary Parkinson’s disease in the Global Parkinson’s Genetics Program (GP2) (npj Parkinsons Disease, (2023), 9, 1, (100), 10.1038/s41531-023-00526-9)
2. Defining the causes of sporadic Parkinson’s disease in the global Parkinson’s genetics program (GP2)
3. Combined genomics and proteomics unveils elusive variants and vast aetiologic heterogeneity in dystonia
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