Authors:
Bruls, T
Gyapay, G
Petit, JL
Artiguenave, F
Vico, V
Qin, SZ
Tin-Wollam, AM
Da Silva, C
Muselet, D
Mavel, D
Pelletier, E
Levy, M
Fujiyama, A
Matsuda, F
Wilson, R
Rowen, L
Hood, L
Weissenbach, J
Saurin, W
Heilig, R
Citation: T. Bruls et al., A physical map of human chromosome 14, NATURE, 409(6822), 2001, pp. 947-948
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:
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:
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