APA (7th ed.) Citation

Ruskey, J. A., Zhou, S., Santiago, R., Franche, L., Alam, A., Roncière, L., . . . Gan‐Or, Z. (2018). The GBA p.Trp378Gly mutation is a probable French‐Canadian founder mutation causing Gaucher disease and synucleinopathies. Clinical Genetics, 94(3/4), 339. https://doi.org/10.1111/cge.13405

Chicago Style (17th ed.) Citation

Ruskey, J. A., et al. "The GBA P.Trp378Gly Mutation Is a Probable French‐Canadian Founder Mutation Causing Gaucher Disease and Synucleinopathies." Clinical Genetics 94, no. 3/4 (2018): 339. https://doi.org/10.1111/cge.13405.

MLA (9th ed.) Citation

Ruskey, J. A., et al. "The GBA P.Trp378Gly Mutation Is a Probable French‐Canadian Founder Mutation Causing Gaucher Disease and Synucleinopathies." Clinical Genetics, vol. 94, no. 3/4, 2018, p. 339, https://doi.org/10.1111/cge.13405.