Berkovic, S. F., Neale, B. M., Zsurka, G., Zizovic, M., Zimprich, F., Zara, F., . . . Chen, S. (2024). Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes. Nature Neuroscience, 27(10), 1864. https://doi.org/10.1038/s41593-024-01747-8
Chicago-referens (17:e uppl.)Berkovic, Samuel F., et al. "Exome Sequencing of 20,979 Individuals with Epilepsy Reveals Shared and Distinct Ultra-rare Genetic Risk Across Disorder Subtypes." Nature Neuroscience 27, no. 10 (2024): 1864. https://doi.org/10.1038/s41593-024-01747-8.
MLA-referens (9:e uppl.)Berkovic, Samuel F., et al. "Exome Sequencing of 20,979 Individuals with Epilepsy Reveals Shared and Distinct Ultra-rare Genetic Risk Across Disorder Subtypes." Nature Neuroscience, vol. 27, no. 10, 2024, p. 1864, https://doi.org/10.1038/s41593-024-01747-8.
