Syrbe, S., & Mütze, U. (2016). Phenotypic variability from benign infantile epilepsy to Ohtahara syndrome associated with a novel mutation in SCN2A. Molecular syndromology, 7(4), . https://doi.org/10.1159/000447526
Chicago-Zitierstil (17. Ausg.)Syrbe, Steffen, und Ulrike Mütze. "Phenotypic Variability from Benign Infantile Epilepsy to Ohtahara Syndrome Associated with a Novel Mutation in SCN2A." Molecular Syndromology 7, no. 4 (2016). https://doi.org/10.1159/000447526.
MLA-Zitierstil (9. Ausg.)Syrbe, Steffen, und Ulrike Mütze. "Phenotypic Variability from Benign Infantile Epilepsy to Ohtahara Syndrome Associated with a Novel Mutation in SCN2A." Molecular Syndromology, vol. 7, no. 4, 2016, https://doi.org/10.1159/000447526.
Achtung: Diese Zitate sind unter Umständen nicht zu 100% korrekt.