APA (7th ed.) Citation

Mathieu, F., Morgan, E., So, J., Munoz, D. G., Mason, W., & Kongkham, P. (2018). Oculoleptomeningeal Amyloidosis Secondary to the Rare Transthyretin c.381T>G (p.Ile127Met) Mutation. World Neurosurgery, 111, 190. https://doi.org/10.1016/j.wneu.2017.12.096

Chicago Style (17th ed.) Citation

Mathieu, Francois, Erin Morgan, Joyce So, David G. Munoz, Warren Mason, and Paul Kongkham. "Oculoleptomeningeal Amyloidosis Secondary to the Rare Transthyretin C.381T>G (p.Ile127Met) Mutation." World Neurosurgery 111 (2018): 190. https://doi.org/10.1016/j.wneu.2017.12.096.

MLA (9th ed.) Citation

Mathieu, Francois, et al. "Oculoleptomeningeal Amyloidosis Secondary to the Rare Transthyretin C.381T>G (p.Ile127Met) Mutation." World Neurosurgery, vol. 111, 2018, p. 190, https://doi.org/10.1016/j.wneu.2017.12.096.