G.P.1.02 Phenotypic spectrum of core-rod myopathy caused by...

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. Romero

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Volume:

Year:

2009

Language:

english

DOI:

10.1016/j.nmd.2009.06.044

File:

PDF, 44 KB

english, 2009

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