Browsing "1. Journal Papers" by Identifier : Dysferlinopathy ; Miyoshi myopathy ; Limb-girdle muscular dystrophy type 2B ; DYSF mutations

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Issue DateTitleJournal Title
2012Two common mutations (p.Gln832X and c.663+1G>C) account for about a third of the DYSF mutations in Korean patients with dysferlinopathyNEUROMUSCULAR DISORDERS
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