Authors: Plaster, NM Tawil, R Tristani-Firouzi, M Canun, S Bendahhou, S Tsunoda, A Donaldson, MR Iannaccone, ST Brunt, E Barohn, R Clark, J Deymeer, F George, AL Fish, FA Hahn, A Nitu, A Ozdemir, C Serdaroglu, P Subramony, SH Wolfe, G Fu, YH Ptacek, LJ

Citation: Nm. Plaster et al., Mutations in Kir2.1 cause the developmental and episodic electrical phenotypes of Andersen's syndrome, CELL, 105(4), 2001, pp. 511-519

Authors: Coffeen, CM McKenna, CE Koeppen, AH Plaster, NM Maragakis, N Mihalopoulos, J Schwankhaus, JD Flanigang, KM Gregg, RG Ptacek, LJ Fu, YH

Citation: Cm. Coffeen et al., Genetic localization of an autosomal dominant leukodystrophy mimicking chronic progressive multiple sclerosis to chromosome 5q31, HUM MOL GEN, 9(5), 2000, pp. 787-793

Authors: Plaster, NM Uyama, E Uchino, M Ikeda, T Flanigan, KM Kondo, I Ptacek, LJ

Citation: Nm. Plaster et al., Genetic localization of the familial adult myoclonic epilepsy (FAME) gene to chromosome 8q24, NEUROLOGY, 53(6), 1999, pp. 1180-1183