Cite
Heterozygous HTRA1 mutations are associated with autosomal dominant cerebral small vessel disease.
MLA
Verdura, Edgard, et al. “Heterozygous HTRA1 Mutations Are Associated with Autosomal Dominant Cerebral Small Vessel Disease.” Brain: A Journal of Neurology, vol. 138, no. 8, Aug. 2015, pp. 2347–58. EBSCOhost, https://doi.org/10.1093/brain/awv155.
APA
Verdura, E., Hervé, D., Scharrer, E., del Mar Amador, M., Guyant-Maréchal, L., Philippi, A., Corlobé, A., Bergametti, F., Gazal, S., Prieto-Morin, C., Beaufort, N., Le Bail, B., Viakhireva, I., Dichgans, M., Chabriat, H., Haffner, C., Tournier-Lasserve, E., Amador, M. D. M., & Bergametti, F. (2015). Heterozygous HTRA1 mutations are associated with autosomal dominant cerebral small vessel disease. Brain: A Journal of Neurology, 138(8), 2347–2358. https://doi.org/10.1093/brain/awv155
Chicago
Verdura, Edgard, Dominique Hervé, Eva Scharrer, Maria del Mar Amador, Lucie Guyant-Maréchal, Anne Philippi, Astrid Corlobé, et al. 2015. “Heterozygous HTRA1 Mutations Are Associated with Autosomal Dominant Cerebral Small Vessel Disease.” Brain: A Journal of Neurology 138 (8): 2347–58. doi:10.1093/brain/awv155.