Abstract
G.P.13.07 Late-onset axial myopathy with cores due to a novel dominant mutation in the skeletal muscle ryanodine receptor (RYR1) gene
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https://doi.org/10.1016/j.nmd.2008.06.292
Journal: Neuromuscular disorders : NMD | Publication Date: Aug 19, 2008 |
G.P.13.07 Late-onset axial myopathy with cores due to a novel dominant mutation in the skeletal muscle ryanodine receptor (RYR1) gene
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