Communicated by Mireille Claustres
Missense mutations in the AFG3L2 proteolytic domain account for ∼1.5% of European autosomal dominant cerebellar ataxias†
Article first published online: 7 SEP 2010
© 2010 Wiley-Liss, Inc.
Volume 31, Issue 10, pages 1117–1124, October 2010
How to Cite
Cagnoli, C., Stevanin, G., Brussino, A., Barberis, M., Mancini, C., Margolis, R. L., Holmes, S. E., Nobili, M., Forlani, S., Padovan, S., Pappi, P., Zaros, C., Leber, I., Ribai, P., Pugliese, L., Assalto, C., Brice, A., Migone, N., Dürr, A. and Brusco, A. (2010), Missense mutations in the AFG3L2 proteolytic domain account for ∼1.5% of European autosomal dominant cerebellar ataxias. Hum. Mutat., 31: 1117–1124. doi: 10.1002/humu.21342
- Issue published online: 28 SEP 2010
- Article first published online: 7 SEP 2010
- Accepted manuscript online: 19 AUG 2010 12:00AM EST
- Manuscript Accepted: 16 JUL 2010
- Manuscript Received: 18 MAR 2010
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