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
published in: American Journal of Human Genetics
date of publication: 2002-10
language: English
main subject: muscular dystrophy, multiminicore myopathy, phenotype
Cites articles 36
- 2001-01-01
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Article - wd:Q24617292