APA (7th ed.) Citation

FL, H., D, W., J, L., M, A., & K, K. (2023). A deep intronic variant in DNM1 in a patient with developmental and epileptic encephalopathy creates a splice acceptor site and affects only transcript variants including exon 10a. Neurogenetics, 24(3), 171. https://doi.org/10.1007/s10048-023-00716-w

Chicago Style (17th ed.) Citation

FL, Harms, Weiss D, Lisfeld J, Alawi M, and Kutsche K. "A Deep Intronic Variant in DNM1 in a Patient with Developmental and Epileptic Encephalopathy Creates a Splice Acceptor Site and Affects Only Transcript Variants Including Exon 10a." Neurogenetics 24, no. 3 (2023): 171. https://doi.org/10.1007/s10048-023-00716-w.

MLA (9th ed.) Citation

FL, Harms, et al. "A Deep Intronic Variant in DNM1 in a Patient with Developmental and Epileptic Encephalopathy Creates a Splice Acceptor Site and Affects Only Transcript Variants Including Exon 10a." Neurogenetics, vol. 24, no. 3, 2023, p. 171, https://doi.org/10.1007/s10048-023-00716-w.