Potential conflict of interest: Nothing to report.
Brief Report
Spinocerebellar ataxia type 12 identified in two Italian families may mimic sporadic ataxia†
Article first published online: 13 APR 2010
DOI: 10.1002/mds.22835
Copyright © 2010 Movement Disorder Society
Additional Information
How to Cite
Brussino, A., Graziano, C., Giobbe, D., Ferrone, M., Dragone, E., Arduino, C., Lodi, R., Tonon, C., Gabellini, A., Rinaldi, R., Miccoli, S., Grosso, E., Bellati, M. C., Orsi, L., Migone, N. and Brusco, A. (2010), Spinocerebellar ataxia type 12 identified in two Italian families may mimic sporadic ataxia. Mov. Disord., 25: 1269–1273. doi: 10.1002/mds.22835
- †
Publication History
- Issue published online: 19 JUL 2010
- Article first published online: 13 APR 2010
- Manuscript Accepted: 13 SEP 2009
- Manuscript Revised: 8 SEP 2009
- Manuscript Received: 13 JUL 2009
Funded by
- Regione Piemonte—Ricerca Sanitaria Finalizzata
- Fondazione Telethon. Grant Number: GGP07110
Cited in:
- CrossRef
This article has been cited by:
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- 2, , , , , , , , , , , Spinocerebellar Ataxias Type 8, 12, and 17 and Dentatorubro-Pallidoluysian Atrophy in Czech Ataxic Patients, The Cerebellum, 2013, 12, 2, 155
- 3, , Recent Advances in the Genetics of Cerebellar Ataxias, Current Neurology and Neuroscience Reports, 2012, 12, 3, 227
- 4, , , , , , Spinocerebellar ataxia type 31 exists in Northeast China, Journal of the Neurological Sciences, 2012, 316, 1-2, 164
- 5, , , Autosomal dominant cerebellar ataxia type I: A review of the phenotypic and genotypic characteristics, Orphanet Journal of Rare Diseases, 2011, 6, 1, 33

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