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Microdeletional mutations of SCN1A in individuals with severe myoclonic epilepsy in infancy (smei) and borderline SMEI 会议论文
27th International Epilepsy Congress, JUL 08-12, 2007
作者:  Wang, J.;  Kurahashi, H.;  Hamachi, A.;  Yonetani, M.;  Inoue, T.
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