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bibliographicCitation Kong Y, Yan K, Hu L, Wang M, Dong X, Lu Y, Wu B, Wang H, Yang L, Zhou W. Association between SCN1A and SCN2A mutations and clinical/EEG features in Chinese patients from epilepsy or severe seizures. Clin Chim Acta. 2018 Aug;483():14–9. doi: 10.1016/j.cca.2018.03.027. PMID: 29649454.
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title Association between SCN1A and SCN2A mutations and clinical/EEG features in Chinese patients from epilepsy or severe seizures
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