Claes L et al. (2003). De novo SCN1A mutations are a major cause of severe myoclonic epilepsy of infancy. Human mutation. 21 [PubMed]

See more from authors: Claes L · Ceulemans B · Audenaert D · Smets K · Löfgren A · Del-Favero J · Ala-Mello S · Basel-Vanagaite L · Plecko B · Raskin S · Thiry P · Wolf NI · Van Broeckhoven C · De Jonghe P

References and models cited by this paper
References and models that cite this paper

Barela AJ et al. (2006). An epilepsy mutation in the sodium channel SCN1A that decreases channel excitability. The Journal of neuroscience : the official journal of the Society for Neuroscience. 26 [PubMed]

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