Authors:
Fonknechten, N
Mavel, D
Byrne, P
Davoine, CS
Cruaud, C
Boentsch, D
Samson, D
Coutinho, P
Hutchinson, M
McMonagle, P
Burgunder, JM
Tartaglione, A
Heinzlef, O
Feki, I
Deufel, T
Parfrey, N
Brice, A
Fontaine, B
Prud'homme, JF
Weissenbach, J
Durr, A
Hazan, J
Citation: N. Fonknechten et al., Spectrum of SPG4 mutations in autosomal dominant spastic paraplegia, HUM MOL GEN, 9(4), 2000, pp. 637-644
Authors:
Zander, C
Yuan, QP
Lindblad, K
Stevanin, G
Durr, A
Davoine, CS
Hazan, J
Fontaine, B
Brice, A
Schalling, M
Citation: C. Zander et al., No evidence for long CAG/CTG repeats in families with spastic paraplegia linked to chromosome 2p21-24, NEUROSCI L, 279(1), 2000, pp. 41-44
Authors:
Lindsey, JC
Lusher, ME
McDermott, CJ
White, KD
Reid, E
Rubinsztein, DC
Bashir, R
Hazan, J
Shaw, PJ
Bushby, KMD
Citation: Jc. Lindsey et al., Mutation analysis of the spastin gene (SPG4) in patients with hereditary spastic paraparesis, J MED GENET, 37(10), 2000, pp. 759-765
Authors:
Fontaine, B
Davoine, CS
Durr, A
Paternotte, C
Feki, I
Weissenbach, J
Hazan, J
Brice, A
Citation: B. Fontaine et al., A new locus for autosomal dominant pure spastic paraplegia, on chromosome 2q24-q34, AM J HU GEN, 66(2), 2000, pp. 702-707
Authors:
Hazan, J
Fonknechten, N
Mavel, D
Paternotte, C
Samson, D
Artiguenave, F
Davoine, CS
Cruaud, C
Durr, A
Wincker, P
Brottier, P
Cattolico, L
Barbe, V
Burgunder, JM
Prud'homme, JF
Brice, A
Fontaine, B
Heilig, R
Weissenbach, J
Citation: J. Hazan et al., Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia, NAT GENET, 23(3), 1999, pp. 296-303
Authors:
Hazan, J
Davoine, CS
Mavel, D
Fonknechten, N
Paternotte, C
Fizames, C
Cruaud, C
Samson, D
Muselet, D
Vega-Czarny, N
Brice, A
Gyapay, G
Heilig, R
Fontaine, B
Weissenbach, J
Citation: J. Hazan et al., A fine integrated map of the SPG4 locus excludes an expanded CAG repeat inchromosome 2p-linked autosomal dominant spastic paraplegia, GENOMICS, 60(3), 1999, pp. 309-319
Authors:
Coutinho, P
Barros, J
Zemmouri, R
Guimaraes, J
Alves, C
Chorao, R
Lourenco, E
Ribeiro, P
Loureiro, JL
Santos, JV
Hamri, A
Paternotte, C
Hazan, J
Silva, MC
Prud'homme, JF
Grid, D
Citation: P. Coutinho et al., Clinical heterogeneity of autosomal recessive spastic paraplegias - Analysis of 106 patients in 46 families, ARCH NEUROL, 56(8), 1999, pp. 943-949
Authors:
Paternotte, C
Rudnicki, D
Fizames, C
Davoine, CS
Mavel, D
Durr, A
Samson, D
Marquette, C
Muselet, D
Vega-Czarny, N
Drouot, N
Voit, T
Fontaine, B
Gyapay, G
Auburger, G
Weissenbach, J
Hazan, J
Citation: C. Paternotte et al., Quality assessment of whole genome mapping data in the refined familial spastic paraplegia interval on chromosome 14q, GENOME RES, 8(11), 1998, pp. 1216-1227