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High frequency of exon 10 mutations in the NOTCH3 gene in Italian CADASIL families: phenotypic peculiarities

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Bibliographic Details
Published in:	Journal of neurology 2010-06, Vol.257 (6), p.1039-1042
Main Authors:	Bianchi, S., Rufa, A., Ragno, M., D’Eramo, C., Pescini, F., Pantoni, L., Cappelli, A., Perretti, A., Zicari, E., Zolo, P., Inzitari, D., Dotti, M. T., Federico, A.
Format:	Article
Language:	English
Subjects:	Adult Aged Aged, 80 and over Biological and medical sciences CADASIL - genetics Cohort Studies Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases DNA Mutational Analysis European Continental Ancestry Group - genetics Exons Family Female Humans Italy Letter to the Editors Male Medical sciences Medicine Medicine & Public Health Middle Aged Mutation Neurology Neuroradiology Neurosciences Pedigree Phenotype Receptor, Notch3 Receptors, Notch - genetics
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