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Results: 2

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
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