Cite
Severe phenotypic spectrum of biallelic mutations in PRRT2 gene.
MLA
Delcourt, Marion, et al. “Severe Phenotypic Spectrum of Biallelic Mutations in PRRT2 Gene.” Journal of Neurology, Neurosurgery & Psychiatry, vol. 86, no. 7, July 2015, pp. 782–85. EBSCOhost, https://doi.org/10.1136/jnnp-2014-309025.
APA
Delcourt, M., Riant, F., Mancini, J., Milh, M., Navarro, V., Roze, E., Humbertclaude, V., Korff, C., Des Portes, V., Szepetowski, P., Doummar, D., Echenne, B., Quintin, S., Leboucq, N., Amrathlal, R. S., Rochette, J., & Roubertie, A. (2015). Severe phenotypic spectrum of biallelic mutations in PRRT2 gene. Journal of Neurology, Neurosurgery & Psychiatry, 86(7), 782–785. https://doi.org/10.1136/jnnp-2014-309025
Chicago
Delcourt, Marion, Florence Riant, Josette Mancini, Mathieu Milh, Vincent Navarro, Emmanuel Roze, Véronique Humbertclaude, et al. 2015. “Severe Phenotypic Spectrum of Biallelic Mutations in PRRT2 Gene.” Journal of Neurology, Neurosurgery & Psychiatry 86 (7): 782–85. doi:10.1136/jnnp-2014-309025.