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Authors: Di Iorio, G Cappa, V Ciccodicola, A Sampaolo, S Ammendola, A Sanges, G Giugliano, R D'Urso, M
Citation: G. Di Iorio et al., A new de novo mutation of the connexin-32 gene in a patient with X-linked Charcot-Marie-Tooth type 1 disease, NEUROL SCI, 21(2), 2000, pp. 109-112

Authors: Sampaolo, S Puca, AA Nigro, V Cappa, V Sannino, V Sanges, G Bonavita, V Di Iorio, G
Citation: S. Sampaolo et al., Lack of sodium channel mutation in an Italian family with paramyotonia congenita, NEUROLOGY, 53(7), 1999, pp. 1549-1555
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