Genetic localization of the familial adult myoclonic epilepsy (FAME) gene to chromosome 8q24
Plaster, N M, Uyama, E, Uchino, M, Ikeda, T, Flanigan, K M, Kondo, I, Ptácek, L J
Published in Neurology (12.10.1999)
Published in Neurology (12.10.1999)
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Genetic localization of an autosomal dominant leukodystrophy mimicking chronic progressive multiple sclerosis to chromosome 5q31
COFFEEN, C. M, MCKENNA, C. E, FU, Y.-H, KOEPPEN, A. H, PLASTER, N. M, MARAGAKIS, N, MIHALOPOULOS, J, SCHWANKHAUS, J. D, FLANIGAN, K. M, GREGG, R. G, PTACEK, L. J
Published in Human molecular genetics (22.03.2000)
Published in Human molecular genetics (22.03.2000)
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Mutations in Kir2.1 Cause the Developmental and Episodic Electrical Phenotypes of Andersen's Syndrome
Plaster, Nikki M., Tawil, Rabi, Tristani-Firouzi, Martin, Canún, Sonia, Bendahhou, Saı̈d, Tsunoda, Akiko, Donaldson, Matthew R., Iannaccone, Susan T., Brunt, Ewout, Barohn, Richard, Clark, John, Deymeer, Feza, George, Alfred L., Fish, Frank A., Hahn, Angelika, Nitu, Alexandru, Ozdemir, Coskun, Serdaroglu, Piraye, Subramony, S.H., Wolfe, Gil, Fu, Ying-Hui, Ptáček, Louis J.
Published in Cell (18.05.2001)
Published in Cell (18.05.2001)
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