Mutations of the selenoprotein N gene, which is implicated in rigid spine muscular dystrophy, cause the classical phenotype of multiminicore disease: reassessing the nosology of early-onset myopathies
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author: Pascale Richard, Ana Ferreiro, Claire Pichereau, Susana Quijano-Roy, Heinz Jungbluth, Francesco Muntoni, Pascale Guicheney, Volker Straub, Carsten G Bönnemann, Michel Fardeau, Jean-Jacques Martin, Nathalie Goemans, Brigitte Estournet
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