DOI:
10.1055/s-00029025
Journal of Pediatric Epilepsy
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References
Claes L, Del-Favero J, Ceulemans B, Lagae L, Van Broeckhoven C, De Jonghe P.
De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancy.
Am J Hum Genet 2001;
68 (6) 1327-1332
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