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	1.	Frequent mutations of SCN1A in severe myoclonic epilepsy in infancy. [electronic resource] by Sugawara, T Mazaki-Miyazaki, E Fukushima, K Shimomura, J Fujiwara, T Hamano, S Inoue, Y Yamakawa, K Producer: 20020507 In: Neurology vol. 58 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Nav1.1 mutations cause febrile seizures associated with afebrile partial seizures. [electronic resource] by Sugawara, T Mazaki-Miyazaki, E Ito, M Nagafuji, H Fukuma, G Mitsudome, A Wada, K Kaneko, S Hirose, S Yamakawa, K Producer: 20010927 In: Neurology vol. 57 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Autosomal dominant epilepsy with febrile seizures plus with missense mutations of the (Na+)-channel alpha 1 subunit gene, SCN1A. [electronic resource] by Ito, M Nagafuji, H Okazawa, H Yamakawa, K Sugawara, T Mazaki-Miyazaki, E Hirose, S Fukuma, G Mitsudome, A Wada, K Kaneko, S Producer: 20020402 In: Epilepsy research vol. 48 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	A missense mutation of the Na+ channel alpha II subunit gene Na(v)1.2 in a patient with febrile and afebrile seizures causes channel dysfunction. [electronic resource] by Sugawara, T Tsurubuchi, Y Agarwala, K L Ito, M Fukuma, G Mazaki-Miyazaki, E Nagafuji, H Noda, M Imoto, K Wada, K Mitsudome, A Kaneko, S Montal, M Nagata, K Hirose, S Yamakawa, K Producer: 20010719 In: Proceedings of the National Academy of Sciences of the United States of America vol. 98 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)