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Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study
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“The G2019S-LRRK2 mutations accounts for 30–41% of all familial cases, and 10% of sporadic PD [23, 31, 38, 39, 57, 58, 68, 99].”
From Cellular and subcellular localization of Rab10 and phospho-T73 Rab10 in the mouse and human brain (2023) · cites this paper as [23]
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Metadata
- Authors
- Healy, D. G., Falchi, M., O'Sullivan, S. S., Bonifati, V., Durr, A., Bressman, S., Brice, A., Aasly, J., Zabetian, C. P., Goldwurm, S., Ferreira, J. J., Tolosa, E., Kay, D. M., Klein, C., Williams, D. R., Marras, C., Lang, A. E., Wszolek, Z. K., Berciano, J., Schapira, A. H., Lynch, T., Bhatia, K. P., Gasser, T., Lees, A. J., & Wood, N. W.
- Venue
- The Lancet Neurology
- Publisher
- Elsevier BV
- Published
- 2008-07
- Volume
- 7
- Issue
- 7
- Pages
- 583-590
- ISSN
- 1474-4422
- PMC
- PMC2832754
- Cited by
- 1,425
- References
- 3
- Language
- en
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