Search Results - "Valcarenghi, C."

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    Neurological features of Fabry disease: clinical, pathophysiological aspects and therapy by Bersano, A., Lanfranconi, S., Valcarenghi, C., Bresolin, N., Micieli, G., Baron, P.

    Published in Acta neurologica Scandinavica (01-08-2012)
    “…Fabry disease is a multisystem, X‐linked, lysosomal storage disorder caused by a mutation in the GLA gene on chromosome Xq22 resulting in alpha‐galactosidase A…”
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    Journal Article