Associated Papers
Genotype-phenotype correlation in PRKN-associated Parkinson's disease.
Menon PJ et al.
Npj Parkinson's Disease, 2024
38553467 (PubMed )
Supplement: 41531_2024_677_MOESM1_ESM.pdf
Intracellular delivery of Parkin-RING0-based fragments corrects Parkin-induced mitochondrial dysfunction through interaction with SLP-2.
Zanon A et al.
Journal of Translational Medicine, 2024
38229174 (PubMed )
Supplement: 12967_2024_4850_MOESM1_ESM.docx
The Role of Rare Coding Variants in Parkinson's Disease GWAS Loci.
Germer EL et al.
Frontiers in Neurology, 2019
31920912 (PubMed )
Supplement: Data_Sheet_1.pdf
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