A novel mutation in FHL1 in a family with X-linked scapuloperoneal myopathy: Phenotypic spectrum and structural study of FHL1 mutations
Keywords: دیستروفی ماهیچهای، دیستروفی عضلانی; X-linked myopathy; Scapuloperoneal; FHL1; Neurogenetics; Muscular dystrophy; Genetic diagnosis;