Ishii, A., Saito, Y., Mitsui, J., Ishiura, H., Yoshimura, J., Arai, H., . . . Hirose, S. (2013). Identification of ATP1A3 Mutations by Exome Sequencing as the Cause of Alternating Hemiplegia of Childhood in Japanese Patients. Public Library of Science.
Citação norma ChicagoIshii, Atsushi, et al. Identification of ATP1A3 Mutations By Exome Sequencing As the Cause of Alternating Hemiplegia of Childhood in Japanese Patients. Public Library of Science, 2013.
Citação norma MLAIshii, Atsushi, et al. Identification of ATP1A3 Mutations By Exome Sequencing As the Cause of Alternating Hemiplegia of Childhood in Japanese Patients. Public Library of Science, 2013.
Nota: a formatação da citação pode não corresponder 100% ao definido pela respectiva norma.