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 - Ferreiro, A; Quijano-Roy, S; Pichereau, C; Moghadaszadeh, B; Goemans, N; Bonnemann, C (Am J Hum Genet, 2002)
et al.