APA (7th ed.) Citation

Chemin, J., Siquier-Pernet, K., Nicouleau, M., Barcia, G., Ahmad, A., Medina-Cano, D., . . . Cantagrel, V. (2018). De novo mutation screening in childhood-onset cerebellar atrophy identifies gain-of-function mutations in the CACNA1G calcium channel gene. Brain (London, England : 1878), 141(7), 1998-2013. https://doi.org/10.1093/brain/awy145

Chicago Style (17th ed.) Citation

Chemin, Jean, et al. "De Novo Mutation Screening in Childhood-onset Cerebellar Atrophy Identifies Gain-of-function Mutations in the CACNA1G Calcium Channel Gene." Brain (London, England : 1878) 141, no. 7 (2018): 1998-2013. https://doi.org/10.1093/brain/awy145.

MLA (9th ed.) Citation

Chemin, Jean, et al. "De Novo Mutation Screening in Childhood-onset Cerebellar Atrophy Identifies Gain-of-function Mutations in the CACNA1G Calcium Channel Gene." Brain (London, England : 1878), vol. 141, no. 7, 2018, pp. 1998-2013, https://doi.org/10.1093/brain/awy145.