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: Guilbot, A Delague, V

Citation: A. Guilbot et V. Delague, From mice to human: periaxin is responsible for an autosomal recessive form of Charcot-Marie-Tooth disease, M S-MED SCI, 17(5), 2001, pp. 663-665

Authors: Salih, MAM Maisonobe, T Kabiraj, M Al Rayess, M Al-Turaiki, MHS Akbar, M Tahan, A Urtizberea, JA Grid, D Hamadouche, T Guilbot, A Brice, A Leguern, E

Citation: Mam. Salih et al., Autosomal recessive hereditary neuropathy with focally folded myelin sheaths and linked to chromosome 11q23: a distinct and homogeneous entity, NEUROMUSC D, 10(1), 2000, pp. 10-15

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: Ring, HZ Chang, H Guilbot, A Brice, A LeGuern, E Francke, U

Citation: Hz. Ring et al., The human neuregulin-2 (NRG2) gene: cloning, mapping and evaluation as a candidate for the autosomal recessive form of Charcot-Marie Tooth disease linked to 5q, HUM GENET, 104(4), 1999, pp. 326-332