Helbig, K. L., Hedrich, U. B., Shinde, D. N., Krey, I., Teichmann, A., Hentschel, J., . . . Lemke, J. R. (2016). A recurrent mutation in KCNA2 as a novel cause of hereditary spastic paraplegia and ataxia. Ann Neurol.
Citação norma ChicagoHelbig, Katherine L., et al. "A Recurrent Mutation in KCNA2 As a Novel Cause of Hereditary Spastic Paraplegia and Ataxia." Ann Neurol 2016.
Citação norma MLAHelbig, Katherine L., et al. "A Recurrent Mutation in KCNA2 As a Novel Cause of Hereditary Spastic Paraplegia and Ataxia." Ann Neurol 2016.
Nota: a formatação da citação pode não corresponder 100% ao definido pela respectiva norma.