S, G., S, O., T, B., F, F., C, B., T, B., . . . RS, M. (2026). Neonatal developmental and epileptic encephalopathy with movement disorder and arthrogryposis: A shared phenotype across brain-expressed sodium channelopathies. Epilepsia, 67(7), 3629. https://doi.org/10.1002/epi.70220
Chicago Style (17th ed.) CitationS, Gverdtsiteli, et al. "Neonatal Developmental and Epileptic Encephalopathy with Movement Disorder and Arthrogryposis: A Shared Phenotype Across Brain-expressed Sodium Channelopathies." Epilepsia 67, no. 7 (2026): 3629. https://doi.org/10.1002/epi.70220.
MLA (9th ed.) CitationS, Gverdtsiteli, et al. "Neonatal Developmental and Epileptic Encephalopathy with Movement Disorder and Arthrogryposis: A Shared Phenotype Across Brain-expressed Sodium Channelopathies." Epilepsia, vol. 67, no. 7, 2026, p. 3629, https://doi.org/10.1002/epi.70220.