![](/img/cover-not-exists.png)
3FC2.2 Muscle MRI in congenital myopathies due to Ryanodine receptor type 1 (RYR1) gene mutations
A. Klein, H. Jungbluth, E. Clement, S. Lillis, S. Abbs, P. Munot, M. Pane, E. Wraige, U. Schara, V. Straub, E.M. Mercuri, F. MuntoniVolume:
15
Year:
2011
Language:
english
Pages:
1
DOI:
10.1016/s1090-3798(11)70096-4
File:
PDF, 36 KB
english, 2011