ObjectiveTo elucidate whether Parkinson’s disease (PD) subtypes show a differential pattern of FP-CIT-SPECT binding during the disease course. MethodsWe examined 27 patients (10 female, 17 male, mean
Rare nonsynonymous variants in autosomal genes in a genome-wide Parkinson’s Disease-relevant gene-set in three unrelated patients with 22q11.2 deletion-associated Parkinson’s disease.
