J.M.W. and S.L. contributed equally to the manuscript.
RYR1 mutations are a common cause of congenital myopathies with central nuclei†
Version of Record online: 13 SEP 2010
Copyright © 2010 American Neurological Association
Annals of Neurology
Volume 68, Issue 5, pages 717–726, November 2010
How to Cite
Wilmshurst, J.M., Lillis, S., Zhou, H., Pillay, K., Henderson, H., Kress, W., Müller, C.R., Ndondo, A., Cloke, V., Cullup, T., Bertini, E., Boennemann, C., Straub, V., Quinlivan, R., Dowling, J.J., Al- Sarraj, S., Treves, S., Abbs, S., Manzur, A.Y., Sewry, C.A., Muntoni, F. and Jungbluth, H. (2010), RYR1 mutations are a common cause of congenital myopathies with central nuclei. Ann Neurol., 68: 717–726. doi: 10.1002/ana.22119
- Issue online: 28 OCT 2010
- Version of Record online: 13 SEP 2010
- Manuscript Revised: 7 JUN 2010
- Manuscript Accepted: 7 JUN 2010
- Manuscript Received: 25 FEB 2010
Additional Supporting Information may be found in the online version of this article.
|ANA_22119_sm_suppinfo1.doc||49K||Supporting Information 1|
|ANA_22119_sm_suppinfo2.doc||29K||Supporting Information 2|
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