![](/img/cover-not-exists.png)
G.P.1.02 Phenotypic spectrum of core-rod myopathy caused by dominant or recessive RYR1 mutations
K.G. Claeys, N. Monnier, P. Laforet, G. Brochier, A. Ferreiro, A. Barois, B. Eymard, J. Lunardi, M. Fardeau, N.B. RomeroVolume:
19
Year:
2009
Language:
english
DOI:
10.1016/j.nmd.2009.06.044
File:
PDF, 44 KB
english, 2009