APA (7th ed.) Citation

KA, M., X, T., I, C., HM, L., BE, W., JA, R., . . . JM, H. (2018). KCTD7 deficiency defines a distinct neurodegenerative disorder with a conserved autophagy-lysosome defect. Annals of neurology, 84(5), 766. https://doi.org/10.1002/ana.25351

Chicago Style (17th ed.) Citation

KA, Metz, et al. "KCTD7 Deficiency Defines a Distinct Neurodegenerative Disorder with a Conserved Autophagy-lysosome Defect." Annals of Neurology 84, no. 5 (2018): 766. https://doi.org/10.1002/ana.25351.

MLA (9th ed.) Citation

KA, Metz, et al. "KCTD7 Deficiency Defines a Distinct Neurodegenerative Disorder with a Conserved Autophagy-lysosome Defect." Annals of Neurology, vol. 84, no. 5, 2018, p. 766, https://doi.org/10.1002/ana.25351.