Actin mutations are one cause of congenital fibre type disproportion
Article first published online: 4 OCT 2004
Copyright © 2003 American Neurological Association
Annals of Neurology
Volume 56, Issue 5, pages 689–694, November 2004
How to Cite
Laing, N. G., Clarke, N. F., Dye, D. E., Liyanage, K., Walker, K. R., Kobayashi, Y., Shimakawa, S., Hagiwara, T., Ouvrier, R., Sparrow, J. C., Nishino, I., North, K. N. and Nonaka, I. (2004), Actin mutations are one cause of congenital fibre type disproportion. Ann Neurol., 56: 689–694. doi: 10.1002/ana.20260
- Issue published online: 25 OCT 2004
- Article first published online: 4 OCT 2004
- Manuscript Accepted: 16 JUL 2004
- Manuscript Revised: 12 JUL 2004
- Manuscript Received: 20 APR 2004
- Australian National Health and Medical Research Council. Grant Numbers: 139170, 139039, 206529
- Association Francaise contre les Myopathies
- West Australian Government Medical and Health Research Infrastructure Fund
- Muscular Dystrophy Association of New South Wales, Australia
- British Heart Foundation
- British Biotechnology and Biological Sciences Research Council
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