Cite
Lesage S, Bras J, Cormier-Dequaire F, et al. Loss-of-function mutations in RAB39B are associated with typical early-onset Parkinson disease. Neurol Genet. 2015;1(1):e9doi: 10.1212/NXG.0000000000000009.
Lesage, S., Bras, J., Cormier-Dequaire, F., Condroyer, C., Nicolas, A., Darwent, L., Guerreiro, R., Majounie, E., Federoff, M., Heutink, P., Wood, N. W., Gasser, T., Hardy, J., Tison, F., Singleton, A., Brice, A. (2015). Loss-of-function mutations in RAB39B are associated with typical early-onset Parkinson disease. Neurology. Genetics, 1(1), e9. https://doi.org/10.1212/NXG.0000000000000009
Lesage, Suzanne, et al. "Loss-of-function mutations in RAB39B are associated with typical early-onset Parkinson disease." Neurology. Genetics vol. 1,1 (2015): e9. doi: https://doi.org/10.1212/NXG.0000000000000009
Lesage S, Bras J, Cormier-Dequaire F, Condroyer C, Nicolas A, Darwent L, Guerreiro R, Majounie E, Federoff M, Heutink P, Wood NW, Gasser T, Hardy J, Tison F, Singleton A, Brice A. Loss-of-function mutations in RAB39B are associated with typical early-onset Parkinson disease. Neurol Genet. 2015 Jun 18;1(1):e9. doi: 10.1212/NXG.0000000000000009. eCollection 2015 Jun. PMID: 27066548; PMCID: PMC4821081.
Copy
Download .nbib