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