PY, W., JX, Z., WH, L., YJ, C., & HW, W. (2026). Toward precision medicine in SCN3A variants-associated encephalopathies and epilepsy: Optimizing genetic diagnosis and molecular subregional effects. Frontiers in neurology, 17, 1772239. https://doi.org/10.3389/fneur.2026.1772239
Chicago Style (17th ed.) CitationPY, Wang, Zhao JX, Liu WH, Chen YJ, and Wang HW. "Toward Precision Medicine in SCN3A Variants-associated Encephalopathies and Epilepsy: Optimizing Genetic Diagnosis and Molecular Subregional Effects." Frontiers in Neurology 17 (2026): 1772239. https://doi.org/10.3389/fneur.2026.1772239.
MLA (9th ed.) CitationPY, Wang, et al. "Toward Precision Medicine in SCN3A Variants-associated Encephalopathies and Epilepsy: Optimizing Genetic Diagnosis and Molecular Subregional Effects." Frontiers in Neurology, vol. 17, 2026, p. 1772239, https://doi.org/10.3389/fneur.2026.1772239.