Recurrent de novo mutations of SCN1A in severe myoclonic epilepsy of infancy.
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U. Stephani | H. Muhle | M. Meisler | A. Siegel | W. Shields | R. RamachandranNair | J. Kearney | A. Wiste | M. Trudeau | R. Elterman | Juliane Reinsdorf | A. Escayg | Anna K. Wiste | R. Ramachandrannair | Miriam H. Meisler | Jennifer A. Kearney | Anna K. Wiste | W. Donald Shields
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