DOI:
10.1055/s-00000041
Neuropediatrics
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References
Ferreiro A, Quijano-Roy S, Pichereau C. , et al.
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.
Am J Hum Genet 2002;
71 (04) 739-749
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