Banuelos, E., Ramsey, K., Belnap, N., Krishnan, M., Balak, C., 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. F1000Res.
Chicago ZitierstilBanuelos, 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." F1000Res 2017.
MLA ZitierstilBanuelos, 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." F1000Res 2017.