Authors:
He, Y
Jones, KJ
Vignier, N
Morgan, G
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Hori, H
Mizuta, T
Tome, FMS
North, KN
Guicheney, P
Citation: Y. He et al., Congenital muscular dystrophy with primary partial laminin alpha 2 chain deficiency: Molecular study, NEUROLOGY, 57(7), 2001, pp. 1319-1322
Authors:
Talim, B
Ferreiro, A
Cormand, B
Vignier, N
Oto, A
Gogus, S
Cila, A
Lehesjoki, AE
Pihko, H
Guicheney, P
Topaloglu, H
Citation: B. Talim et al., Merosin-deficient congenital muscular dystrophy with mental retardation and cerebellar cysts unlinked to the LAMA2, FCMD and MEB loci, NEUROMUSC D, 10(8), 2000, pp. 548-552
Authors:
Di Blasi, C
Mora, M
Pareyson, D
Farina, L
Sghirlanzoni, A
Vignier, N
Blasevich, F
Cornelio, F
Guicheney, P
Morandi, L
Citation: C. Di Blasi et al., Partial laminin alpha 2 chain deficiency in a patient with myopathy resembling inclusion body myositis, ANN NEUROL, 47(6), 2000, pp. 811-816
Authors:
Neyroud, N
Richard, P
Vignier, N
Donger, C
Denjoy, I
Demay, L
Shkolnikova, M
Pesce, R
Chevalier, P
Hainque, B
Coumel, P
Schwartz, K
Guicheney, P
Citation: N. Neyroud et al., Genomic organization of the KCNQ1 K+ channel gene and identification of C-terminal mutations in the long-QT syndrome, CIRCUL RES, 84(3), 1999, pp. 290-297
Authors:
Vignier, N
Moghadaszadeh, B
Gary, F
Beckmann, J
Mayer, U
Guicheney, P
Citation: N. Vignier et al., Structure, genetic localization, and identification of the cardiac and skeletal muscle transcripts of the human integrin alpha 7 gene (ITGA7), BIOC BIOP R, 260(2), 1999, pp. 357-364