Authors:
Gaspar, C
Lopes-Cendes, I
Hayes, S
Goto, J
Arvidsson, K
Dias, A
Silveira, I
Maciel, P
Coutinho, P
Lima, M
Zhou, YX
Soong, BW
Watanabe, M
Giunti, P
Stevanin, G
Riess, O
Sasaki, H
Hsieh, M
Nicholson, GA
Brunt, E
Higgins, JJ
Lauritzen, M
Tranebjaerg, L
Volpini, V
Wood, N
Ranum, L
Tsuji, S
Brice, A
Sequeiros, J
Rouleau, GA
Citation: C. Gaspar et al., Ancestral origins of the Machado-Joseph disease mutation: A worldwide haplotype study, AM J HU GEN, 68(2), 2001, pp. 523-528
Authors:
Stevanin, G
David, G
Durr, A
Giunti, P
Benomar, A
Abada-Bendib, M
Lee, MS
Agid, Y
Brice, A
Citation: G. Stevanin et al., Multiple origins of the spinocerebellar ataxia 7 (SCA7) mutation revealed by linkage disequilibrium studies with closely flanking markers, including an intragenic polymorphism (G(3145)TG/A(3145)TG), EUR J HUM G, 7(8), 1999, pp. 889-896
Authors:
Worth, PF
Giunti, P
Gardner-Thorpe, C
Dixon, PH
Davis, MB
Wood, NW
Citation: Pf. Worth et al., Autosomal dominant cerebellar ataxia type III: Linkage in a large British family to a 7.6-cM region on chromosome 15q14-21.3, AM J HU GEN, 65(2), 1999, pp. 420-426
Authors:
Giunti, P
Stevanin, G
Worth, PF
David, G
Brice, A
Wood, NW
Citation: P. Giunti et al., Molecular and clinical study of 18 families with ADCA type II: Evidence for genetic heterogeneity and De Novo mutation, AM J HU GEN, 64(6), 1999, pp. 1594-1603