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Four new Finnish families with LGMD1D; refinement of the clinical phenotype and the linked 7q36 locus.Hackman P et al. Neuromuscul Disord. (2011)
Untangling the complexity of limb-girdle muscular dystrophies.Liewluck T et al. Muscle Nerve. (2018)
Novel mutation identification and copy number variant detection via exome sequencing in congenital muscular dystrophy.Cauley ES et al. Mol Genet Genomic Med. (2020)
Date introduced: August 25, 2010
MeSH Unique ID: C535906
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