Associated Papers
RAB32 Ser71Arg in autosomal dominant Parkinson's disease: linkage, association, and functional analyses.
Gustavsson EK et al.
The Lancet. Neurology, 2024
38614108 (PubMed )
Supplement: NIHMS1992133-supplement-Suppl__Appendix_II.xlsx › page_4
A pathogenic variant in RAB32 causes autosomal dominant Parkinson's disease and activates LRRK2 kinase.
Gustavsson EK et al.
Medrxiv : the Preprint Server for Health Sciences, 2024
38293014 (PubMed )
Supplement: media-1.pdf
LowMACA: exploiting protein family analysis for the identification of rare driver mutations in cancer.
Melloni GE et al.
Bmc Bioinformatics, 2016
26860319 (PubMed )
Supplement: 12859_2016_935_MOESM2_ESM.xlsx › Table_S5
Select a paper to view details