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G.P.13.07 Late-onset axial myopathy with cores due to a novel dominant mutation in the skeletal muscle ryanodine receptor (RYR1) gene

✍ Scribed by H. Jungbluth; S. Lillis; H. Zhou; S. Abbs; M. Swash; F. Muntoni

No coin nor oath required. For personal study only.

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