APA (7th ed.) Citation

Deschauer, M., Hengel, H., Rupprich, K., Kreiß, M., Schlotter-Weigel, B., Grimmel, M., . . . Haack, T. B. (2021). Bi-allelic truncating mutations in VWA1 cause neuromyopathy. Brain, 144(2), . https://doi.org/10.1093/brain/awaa418

Chicago Style (17th ed.) Citation

Deschauer, Marcus, et al. "Bi-allelic Truncating Mutations in VWA1 Cause Neuromyopathy." Brain 144, no. 2 (2021). https://doi.org/10.1093/brain/awaa418.

MLA (9th ed.) Citation

Deschauer, Marcus, et al. "Bi-allelic Truncating Mutations in VWA1 Cause Neuromyopathy." Brain, vol. 144, no. 2, 2021, https://doi.org/10.1093/brain/awaa418.