Loss-of-function mutations in RAB39B are associated with typical early-onset Parkinson disease.

MLA

Lesage, Suzanne, et al. “Loss-of-Function Mutations in RAB39B Are Associated with Typical Early-Onset Parkinson Disease.” Neurology. Genetics, vol. 1, no. 1, June 2015, p. e9. EBSCOhost, https://doi.org/10.1212/NXG.0000000000000009.

APA

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

Chicago

Lesage, Suzanne, Jose Bras, Florence Cormier-Dequaire, Christel Condroyer, Aude Nicolas, Lee Darwent, Rita Guerreiro, et al. 2015. “Loss-of-Function Mutations in RAB39B Are Associated with Typical Early-Onset Parkinson Disease.” Neurology. Genetics 1 (1): e9. doi:10.1212/NXG.0000000000000009.