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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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Description scientific article
Author/s

author: Ana Ferreiro  Carsten G Bönnemann  Susana Quijano-Roy  Volker Straub  Jean-Jacques Martin  Nathalie Goemans  Michel Fardeau  Heinz Jungbluth  Claire Pichereau  Francesco Muntoni  Brigitte Estournet  Pascale Richard  Pascale Guicheney 

Publication date October 2002
Language English
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