Genes for autosomal recessive cerebellar ataxia: order from chaos? অনুযায়ী Nemeth, A, Dunne, E, Bomont, P, Moreira, M, Bochukova, E, Huson, S, Taylor, A, Koenig, M

Autosomal recessive ataxias: a new gene - aprataxin - responsible for ataxia-ocular apraxia 1, and a new locus on 9q34 অনুযায়ী Moreira, M, Klur, S, Barbot, C, Tachi, N, Bomont, P, Watanabe, M, Shoji, M, Warter, J, Aubourg, P, Durr, A, Nemeth, A, Amouri, R, Hentati, F, Alurkar, A, Divekar, D, Mendoca, P, Sequeiros, J, Coutinho, P, Koenig, M

Senataxin, the ortholog of a yeast RNA helicase, is mutant in ataxia-ocular apraxia 2. অনুযায়ী Moreira, M, Klur, S, Watanabe, M, Németh, A, Le Ber, I, Moniz, J, Tranchant, C, Aubourg, P, Tazir, M, Schöls, L, Pandolfo, M, Schulz, J, Pouget, J, Calvas, P, Shizuka-Ikeda, M, Shoji, M, Tanaka, M, Izatt, L, Shaw, C, M'Zahem, A, Dunne, E, Bomont, P, Benhassine, T, Bouslam, N, Stevanin, G

Mutations in the beta-tubulin gene TUBB2B result in asymmetrical polymicrogyria. অনুযায়ী Jaglin, X, Poirier, K, Saillour, Y, Buhler, E, Tian, G, Bahi-Buisson, N, Fallet-Bianco, C, Phan-Dinh-Tuy, F, Kong, X, Bomont, P, Castelnau-Ptakhine, L, Odent, S, Loget, P, Kossorotoff, M, Snoeck, I, Plessis, G, Parent, P, Beldjord, C, Cardoso, C, Represa, A, Flint, J, Keays, D, Cowan, N, Chelly, J