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3FC2.2 Muscle MRI in congenital myopathies due to Ryanodine receptor type 1 (RYR1) gene mutations

✍ Scribed by A. Klein; H. Jungbluth; E. Clement; S. Lillis; S. Abbs; P. Munot; M. Pane; E. Wraige; U. Schara; V. Straub; E.M. Mercuri; F. Muntoni

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