AAAAAA

   
Results: 1-4 |
Results: 4

Authors: Guilbot, A Williams, A Ravise, N Verny, C Brice, A Sherman, DL Brophy, PJ LeGuern, E Delague, V Bareil, C Megarbane, A Claustres, M
Citation: A. Guilbot et al., A mutation in periaxin is responsible for CMT4F, an autosomal recessive form of Charcot-Marie-Tooth disease, HUM MOL GEN, 10(4), 2001, pp. 415-421

Authors: Lebre, AS Jamot, L Takahashi, J Spassky, N Leprince, C Ravise, N Zander, C Fujigasaki, H Kussel-Andermann, P Duyckaerts, C Camonis, JH Brice, A
Citation: As. Lebre et al., Ataxin-7 interacts with a Cbl-associated protein that it recruits into neuronal intranuclear inclusions, HUM MOL GEN, 10(11), 2001, pp. 1201-1213

Authors: Guilbot, A Ravise, N Bouhouche, A Coullin, P Birouk, N Maisonobe, T Kuntzer, T Vial, C Grid, D Brice, A LeGuern, E
Citation: A. Guilbot et al., Genetic, cytogenetic and physical refinement of the autosomal recessive CMT linked to 5q31-q33: exclusion of candidate genes including EGR1, EUR J HUM G, 7(8), 1999, pp. 849-859

Authors: Coullin, P Philippe, C Ravise, N Bernheim, A
Citation: P. Coullin et al., Simultaneous fluorescence in-situ hybridization (FISH) and R-banding by primed in-situ labelling (PRINS), CHROMOS RES, 7(3), 1999, pp. 241-242
Risultati: 1-4 |