Purkinje cell mitochondrial oxidative defect in the animal model of spinocerebellar ataxia type 1 Clinical and pathological aspects of an Italian patient with inclusion body myopathy and frontotemporal dementia carrying a novel mutation in valosin-containing protein gene.
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Data di Pubblicazione:
2007
Citazione:
Purkinje cell mitochondrial oxidative defect in the animal model of spinocerebellar
ataxia type 1
Clinical and pathological aspects of an Italian patient with inclusion body myopathy and frontotemporal dementia carrying a novel mutation in valosin-containing protein gene / V. Lucchini, G. Fagiolari, C. Lamperti, F. Fortunato, D. Ponzi, V. Crugnola, M. Sciacco, N. Bresolin, M. Moggio, G.P. Comi, S. Bonato. ((Intervento presentato al convegno 17° Meeting of the European Neurological Society tenutosi a null nel null.
Tipologia IRIS:
14 - Intervento a convegno non pubblicato
Elenco autori:
V. Lucchini, G. Fagiolari, C. Lamperti, F. Fortunato, D. Ponzi, V. Crugnola, M. Sciacco, N. Bresolin, M. Moggio, G.P. Comi, S. Bonato
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