Authors: Seznec, H Agbulut, O Sergeant, N Savouret, C Ghestem, A Tabti, N Willer, JC Ourth, L Duros, C Brisson, E Fouquet, C Butler-Browne, G Delacourte, A Junien, C Gourdon, G

Citation: H. Seznec et al., Mice transgenic for the human myotonic dystrophy region with expanded CTG repeats display muscular and brain abnormalities, HUM MOL GEN, 10(23), 2001, pp. 2717-2726

Authors: Fontaine, B Tabti, N

Citation: B. Fontaine et N. Tabti, Ionic channels and channels diseases: molecular and functional relationships, M S-MED SCI, 17(10), 2001, pp. 967-968

Authors: Sternberg, D Maisonobe, T Jurkat-Rott, K Nicole, S Launay, E Chauveau, D Tabti, N Lehmann-Horn, F Hainque, B Fontaine, B

Citation: D. Sternberg et al., Hypokalaemic periodic paralysis type 2 caused by mutations at codon 672 inthe muscle sodium channel gene SCN4A, BRAIN, 124, 2001, pp. 1091-1099

Authors: Fontaine, B Tabti, N

Citation: B. Fontaine et N. Tabti, Unravelling the pathophysiology of calcium channel mutations causing neurological disorders, BRAIN, 123, 2000, pp. 423-424