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Filters: Keyword is Muscular Dystrophies, Limb-Girdle and Author is Mroczek, Magdalena [Clear All Filters]
Four Individuals with a Homozygous Mutation in Exon 1f of the Gene and Associated Myasthenic Features. Genes (Basel) 11, (2020).
Sequential targeted exome sequencing of 1001 patients affected by unexplained limb-girdle weakness. Genet Med 22, 1478-1488 (2020).