Résultats de la recherche

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Impacts of massively parallel sequencing for genetic diagnosis of neuromuscular disorders
VaRank: a simple and powerful tool for ranking genetic variants
Altered splicing of the BIN1 muscle-specific exon in humans and dogs with highly progressive centronuclear myopathy
Next generation sequencing for molecular diagnosis of neuromuscular diseases
Recessive mutations in the kinase ZAK cause a congenital myopathy with fibre type disproportion

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