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