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	1.	Genetic localization of the familial adult myoclonic epilepsy (FAME) gene to chromosome 8q24. [electronic resource] by Plaster, N M Uyama, E Uchino, M Ikeda, T Flanigan, K M Kondo, I Ptácek, L J Producer: 19991217 In: Neurology vol. 53 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Genetic localization of an autosomal dominant leukodystrophy mimicking chronic progressive multiple sclerosis to chromosome 5q31. [electronic resource] by Coffeen, C M McKenna, C E Koeppen, A H Plaster, N M Maragakis, N Mihalopoulos, J Schwankhaus, J D Flanigan, K M Gregg, R G Ptácek, L J Fu, Y H Producer: 20000601 In: Human molecular genetics vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Mutations in Kir2.1 cause the developmental and episodic electrical phenotypes of Andersen's syndrome. [electronic resource] by Plaster, N M Tawil, R Tristani-Firouzi, M Canún, S Bendahhou, S Tsunoda, A Donaldson, M R Iannaccone, S T Brunt, E Barohn, R Clark, J Deymeer, F George, A L Fish, F A Hahn, A Nitu, A Ozdemir, C Serdaroglu, P Subramony, S H Wolfe, G Fu, Y H Ptácek, L J Producer: 20010705 In: Cell vol. 105 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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