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Results: 1-3 |
Results: 3

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: Gaspar, C Lopes-Cendes, I Hayes, S Goto, J Arvidsson, K Dias, A Silveira, I Maciel, P Coutinho, P Lima, M Zhou, YX Soong, BW Watanabe, M Giunti, P Stevanin, G Riess, O Sasaki, H Hsieh, M Nicholson, GA Brunt, E Higgins, JJ Lauritzen, M Tranebjaerg, L Volpini, V Wood, N Ranum, L Tsuji, S Brice, A Sequeiros, J Rouleau, GA
Citation: C. Gaspar et al., Ancestral origins of the Machado-Joseph disease mutation: A worldwide haplotype study, AM J HU GEN, 68(2), 2001, pp. 523-528

Authors: Niemela, O Parkkila, S Britton, RS Brunt, E Janney, C Bacon, B
Citation: O. Niemela et al., Hepatic lipid peroxidation in hereditary hemochromatosis and alcoholic liver injury, J LA CL MED, 133(5), 1999, pp. 451-460
Risultati: 1-3 |