Order Article Reprints

Zhu Z, Bolt E, Newmaster K, Osei-Bonsu W, Cohen S, Cuddapah VA, Gupta S, Paudel S, Samanta D, Dang LT, et al. SCN1B Genetic Variants: A Review of the Spectrum of Clinical Phenotypes and a Report of Early Myoclonic Encephalopathy. Children. 2022; 9(10):1507. https://doi.org/10.3390/children9101507

Zhu, Zahra, Elizabeth Bolt, Kyra Newmaster, Wendy Osei-Bonsu, Stacey Cohen, Vishnu Anand Cuddapah, Siddharth Gupta, Sita Paudel, Debopam Samanta, Louis T. Dang, and et al. 2022. "SCN1B Genetic Variants: A Review of the Spectrum of Clinical Phenotypes and a Report of Early Myoclonic Encephalopathy" Children 9, no. 10: 1507. https://doi.org/10.3390/children9101507

Zhu, Z., Bolt, E., Newmaster, K., Osei-Bonsu, W., Cohen, S., Cuddapah, V. A., Gupta, S., Paudel, S., Samanta, D., Dang, L. T., Carney, P. R., & Naik, S. (2022). SCN1B Genetic Variants: A Review of the Spectrum of Clinical Phenotypes and a Report of Early Myoclonic Encephalopathy. Children, 9(10), 1507. https://doi.org/10.3390/children9101507