A recessive form of central core disease, transiently presenting as multi-minicore disease, is associated with a homozygous mutation in the ryanodine receptor type 1 gene
Article first published online: 21 MAY 2002
Copyright © 2002 Wiley-Liss, Inc.
Annals of Neurology
Volume 51, Issue 6, pages 750–759, June 2002
How to Cite
Ferreiro, A., Monnier, N., Romero, N. B., Leroy, J.-P., Bönnemann, C., Haenggeli, C.-A., Straub, V., Voss, W. D., Nivoche, Y., Jungbluth, H., Lemainque, A., Voit, T., Lunardi, J., Fardeau, M. and Guicheney, P. (2002), A recessive form of central core disease, transiently presenting as multi-minicore disease, is associated with a homozygous mutation in the ryanodine receptor type 1 gene. Ann Neurol., 51: 750–759. doi: 10.1002/ana.10231
- Issue published online: 21 MAY 2002
- Article first published online: 21 MAY 2002
- Manuscript Accepted: 28 FEB 2002
- Manuscript Revised: 21 FEB 2002
- Manuscript Received: 26 DEC 2001
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