Authors:
He, Y
Jones, KJ
Vignier, N
Morgan, G
Chevallay, M
Barois, A
Estournet-Mathiaud, B
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:
Fardeau, M
Vicart, P
Caron, A
Chateau, D
Chevallay, M
Collin, H
Chapon, F
Duboc, D
Eymard, B
Tome, FMS
Dupret, JM
Paulin, D
Guicheney, P
Citation: M. Fardeau et al., Familial myopathy with desmin storage seen as a granulo-filamentar, electron-dense material with mutation of the alpha beta-cristallin gene, REV NEUROL, 156(5), 2000, pp. 497-504