P.P.5 02 Muscle MRI in a family with congenital myopathy with cores and rods associated with a novel missense mutation in the ryanodine receptor 1 gene

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Bibliographic Details
Published in:Neuromuscular disorders : NMD 2006-10, Vol.16 (9), p.687-688
Main Authors: von der Hagen, M., Kaindl, A.M., Kress, W., Mitzscherling, P., Hübner, A., Reible, C.R., Hahn, G., Stoltenburg-Didinger, G.
Format: Article
Language:English
Online Access:Get full text
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ISSN:0960-8966
1873-2364
DOI:10.1016/j.nmd.2006.05.147