Campostrini, G., DiFrancesco, J. C., Castellotti, B., Milanesi, R., Gnecchi-Ruscone, T., Bonzanni, M., . . . DiFrancesco, D. (2018). A Loss-of-Function HCN4 Mutation Associated With Familial Benign Myoclonic Epilepsy in Infancy Causes Increased Neuronal Excitability. Front Mol Neurosci.
Chicago ZitierstilCampostrini, Giulia, et al. "A Loss-of-Function HCN4 Mutation Associated With Familial Benign Myoclonic Epilepsy in Infancy Causes Increased Neuronal Excitability." Front Mol Neurosci 2018.
MLA ZitierstilCampostrini, Giulia, et al. "A Loss-of-Function HCN4 Mutation Associated With Familial Benign Myoclonic Epilepsy in Infancy Causes Increased Neuronal Excitability." Front Mol Neurosci 2018.
Achtung: Diese Zitate sind unter Umständen nicht zu 100% korrekt.