Genetic etiology of Parkinson disease associated with mutations in the SNCA, PARK2, PINK1, PARK7, and LRRK2 genes: a mutation update.

MLA

Nuytemans, Karen, et al. “Genetic Etiology of Parkinson Disease Associated with Mutations in the SNCA, PARK2, PINK1, PARK7, and LRRK2 Genes: A Mutation Update.” Human Mutation, vol. 31, no. 7, July 2010, pp. 763–80. EBSCOhost, https://doi.org/10.1002/humu.21277.

APA

Nuytemans, K., Theuns, J., Cruts, M., & Van Broeckhoven, C. (2010). Genetic etiology of Parkinson disease associated with mutations in the SNCA, PARK2, PINK1, PARK7, and LRRK2 genes: a mutation update. Human Mutation, 31(7), 763–780. https://doi.org/10.1002/humu.21277

Chicago

Nuytemans, Karen, Jessie Theuns, Marc Cruts, and Christine Van Broeckhoven. 2010. “Genetic Etiology of Parkinson Disease Associated with Mutations in the SNCA, PARK2, PINK1, PARK7, and LRRK2 Genes: A Mutation Update.” Human Mutation 31 (7): 763–80. doi:10.1002/humu.21277.