Authors:
Puccio, H
Simon, D
Cossee, M
Criqui-Filipe, P
Tiziano, F
Melki, J
Hindelang, C
Matyas, R
Rustin, P
Koenig, M
Citation: H. Puccio et al., Mouse models for Friedreich ataxia exhibit cardiomyopathy, sensory nerve defect and Fe-S enzyme deficiency followed by intramitochondrial iron deposits, NAT GENET, 27(2), 2001, pp. 181-186
Authors:
Cossee, M
Puccio, H
Gansmuller, A
Koutnikova, H
Dierich, A
LeMeur, M
Fischbeck, K
Dolle, P
Koenig, M
Citation: M. Cossee et al., Inactivation of the Friedreich ataxia mouse gene leads to early embryonic lethality without iron accumulation, HUM MOL GEN, 9(8), 2000, pp. 1219-1226
Authors:
Cossee, M
Durr, A
Schmitt, M
Dahl, N
Trouillas, P
Allinson, P
Kostrzewa, M
Nivelon-Chevallier, A
Gustavson, KH
Kohlschutter, A
Muller, U
Mandel, JL
Brice, A
Koenig, M
Cavalcanti, F
Tammaro, A
De Michele, G
Filla, A
Cocozza, S
Labuda, M
Montermini, L
Poirier, J
Pandolfo, M
Citation: M. Cossee et al., Friedreich's ataxia: Point mutations and clinical presentation of compoundheterozygotes, ANN NEUROL, 45(2), 1999, pp. 200-206
Authors:
Delatycki, MB
Knight, M
Koenig, M
Cossee, M
Williamson, R
Forrest, SM
Citation: Mb. Delatycki et al., G130V, a common FRDA point mutation, appears to have arisen from a common founder, HUM GENET, 105(4), 1999, pp. 343-346