APA (7th ed.) Citation

Huin, V., Barbier, M., Bottani, A., Lobrinus, J. A., Clot, F., Lamari, F., . . . Durr, A. (2019). Homozygous GRN mutations: New phenotypes and new insights into pathological and molecular mechanisms. Brain: A Journal of Neurology, 142(1), 303. https://doi.org/10.1093/brain/awz377

Chicago Style (17th ed.) Citation

Huin, Vincent, et al. "Homozygous GRN Mutations: New Phenotypes and New Insights into Pathological and Molecular Mechanisms." Brain: A Journal of Neurology 142, no. 1 (2019): 303. https://doi.org/10.1093/brain/awz377.

MLA (9th ed.) Citation

Huin, Vincent, et al. "Homozygous GRN Mutations: New Phenotypes and New Insights into Pathological and Molecular Mechanisms." Brain: A Journal of Neurology, vol. 142, no. 1, 2019, p. 303, https://doi.org/10.1093/brain/awz377.