APA (7th ed.) Citation

Banuelos, E., Ramsey, K., Belnap, N., Krishnan, M., Balak, C. D., Szelinger, S., . . . Schrauwen, I. (2017). Case Report: Novel mutations in TBC1D24 are associated with autosomal dominant tonic-clonic and myoclonic epilepsy and recessive Parkinsonism, psychosis, and intellectual disability. F1000 research, 6, 553. https://doi.org/10.12688/f1000research.10588.1

Chicago Style (17th ed.) Citation

Banuelos, Erika, et al. "Case Report: Novel Mutations in TBC1D24 Are Associated with Autosomal Dominant Tonic-clonic and Myoclonic Epilepsy and Recessive Parkinsonism, Psychosis, and Intellectual Disability." F1000 Research 6 (2017): 553. https://doi.org/10.12688/f1000research.10588.1.

MLA (9th ed.) Citation

Banuelos, Erika, et al. "Case Report: Novel Mutations in TBC1D24 Are Associated with Autosomal Dominant Tonic-clonic and Myoclonic Epilepsy and Recessive Parkinsonism, Psychosis, and Intellectual Disability." F1000 Research, vol. 6, 2017, p. 553, https://doi.org/10.12688/f1000research.10588.1.