Claes L et al. (2001). De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancy. American journal of human genetics. 68 [PubMed]

See more from authors: Claes L · Del-Favero J · Ceulemans B · Lagae L · 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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