Evely, K. M., Pryce, K. D., & Bhattacharjee, A. (2017). The Phe932Ile mutation in KCNT1 channels associated with severe epilepsy, delayed myelination and leukoencephalopathy produces a loss-of-function channel phenotype. Neuroscience.
Trích dẫn kiểu ChicagoEvely, Katherine M., Kerri D. Pryce, và Arin Bhattacharjee. "The Phe932Ile Mutation in KCNT1 Channels Associated With Severe Epilepsy, Delayed Myelination and Leukoencephalopathy Produces a Loss-of-function Channel Phenotype." Neuroscience 2017.
Trích dẫn MLAEvely, Katherine M., Kerri D. Pryce, và Arin Bhattacharjee. "The Phe932Ile Mutation in KCNT1 Channels Associated With Severe Epilepsy, Delayed Myelination and Leukoencephalopathy Produces a Loss-of-function Channel Phenotype." Neuroscience 2017.