APA (7th ed.) Citation

M, P., J, J., V, R., L, L., D, G., C, T., . . . K, F. (2019). A novel missense variant in SLC18A2 causes recessive brain monoamine vesicular transport disease and absent serotonin in platelets. JIMD reports, 47(1), 9. https://doi.org/10.1002/jmd2.12030

Chicago Style (17th ed.) Citation

M, Padmakumar, et al. "A Novel Missense Variant in SLC18A2 Causes Recessive Brain Monoamine Vesicular Transport Disease and Absent Serotonin in Platelets." JIMD Reports 47, no. 1 (2019): 9. https://doi.org/10.1002/jmd2.12030.

MLA (9th ed.) Citation

M, Padmakumar, et al. "A Novel Missense Variant in SLC18A2 Causes Recessive Brain Monoamine Vesicular Transport Disease and Absent Serotonin in Platelets." JIMD Reports, vol. 47, no. 1, 2019, p. 9, https://doi.org/10.1002/jmd2.12030.