Phenotypic Variability from Benign Infantile Epilepsy to Ohtahara Syndrome Associated with a Novel Mutation in SCN2A .

MLA

Syrbe, Steffen, et al. “Phenotypic Variability from Benign Infantile Epilepsy to Ohtahara Syndrome Associated with a Novel Mutation in SCN2A .” Molecular Syndromology, vol. 7, no. 4, Sept. 2016, pp. 182–88. EBSCOhost, https://doi.org/10.1159/000447526.

APA

Syrbe, S., Zhorov, B. S., Bertsche, A., Bernhard, M. K., Hornemann, F., Mütze, U., Hoffmann, J., Hörtnagel, K., Kiess, W., Hirsch, F. W., Lemke, J. R., & Merkenschlager, A. (2016). Phenotypic Variability from Benign Infantile Epilepsy to Ohtahara Syndrome Associated with a Novel Mutation in SCN2A . Molecular Syndromology, 7(4), 182–188. https://doi.org/10.1159/000447526

Chicago

Syrbe, Steffen, Boris S Zhorov, Astrid Bertsche, Matthias K Bernhard, Frauke Hornemann, Ulrike Mütze, Jessica Hoffmann, et al. 2016. “Phenotypic Variability from Benign Infantile Epilepsy to Ohtahara Syndrome Associated with a Novel Mutation in SCN2A .” Molecular Syndromology 7 (4): 182–88. doi:10.1159/000447526.