Novel CCM2 missense variants abrogating the CCM1-CCM2 interaction cause cerebral cavernous malformations.

MLA

Bergametti, Françoise, et al. “Novel CCM2 Missense Variants Abrogating the CCM1-CCM2 Interaction Cause Cerebral Cavernous Malformations.” Journal of Medical Genetics, vol. 57, no. 6, June 2020, pp. 400–04. EBSCOhost, https://doi.org/10.1136/jmedgenet-2019-106401.

APA

Bergametti, F., Viot, G., Verny, C., Brechard, M. P., Denier, C., Labauge, P., Petit, P., Nouet, A., Viallet, F., Chaussenot, A., Hervé, D., Tournier-Lasserve, E., & Riant, F. (2020). Novel CCM2 missense variants abrogating the CCM1-CCM2 interaction cause cerebral cavernous malformations. Journal of Medical Genetics, 57(6), 400–404. https://doi.org/10.1136/jmedgenet-2019-106401

Chicago

Bergametti, Françoise, Geraldine Viot, Christophe Verny, Marie Pierre Brechard, Christian Denier, Pierre Labauge, Paul Petit, et al. 2020. “Novel CCM2 Missense Variants Abrogating the CCM1-CCM2 Interaction Cause Cerebral Cavernous Malformations.” Journal of Medical Genetics 57 (6): 400–404. doi:10.1136/jmedgenet-2019-106401.