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
Exome sequencing identifies a spectrum of mutation frequencies in advanced and lethal prostate cancers.
Kumar A et al.
Proceedings of the National Academy of Sciences of the United States of America, 2011
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