Naderian, R., Vafaeian, F., Hoseini, S. M., & Sanami, S. (2025). Case report of Lafora disease: A rare genetic disorder manifesting as progressive myoclonic epilepsy. BMC neurology, 25(1), 230-6. https://doi.org/10.1186/s12883-025-04253-x
Citace podle Chicago (17th ed.)Naderian, Ramtin, Farzane Vafaeian, Seyyed Mohamad Hoseini, a Samira Sanami. "Case Report of Lafora Disease: A Rare Genetic Disorder Manifesting as Progressive Myoclonic Epilepsy." BMC Neurology 25, no. 1 (2025): 230-6. https://doi.org/10.1186/s12883-025-04253-x.
Citace podle MLA (9th ed.)Naderian, Ramtin, et al. "Case Report of Lafora Disease: A Rare Genetic Disorder Manifesting as Progressive Myoclonic Epilepsy." BMC Neurology, vol. 25, no. 1, 2025, pp. 230-6, https://doi.org/10.1186/s12883-025-04253-x.