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