Citation Tools
PDF
Other content recommended for you
- Making sense of the clinical spectrum of limb girdle muscular dystrophies
- Muscle disease
- Patients with a phenotype consistent with facioscapulohumeral muscular dystrophy display genetic and epigenetic heterogeneity
- Diagnosis and management of the limb girdle muscular dystrophies
- Respiratory involvement in inherited primary muscle conditions
- Screening of calpain-3 autolytic activity in LGMD muscle: a functional map of CAPN3 gene mutations
- Muscle diseases: mimics and chameleons
- Extension of the clinical range of facioscapulohumeral dystrophy: report of six cases
- EVALUATING MUSCLE SYMPTOMS
- Frequency of dystrophic muscle abnormalities in chronic progressive external ophthalmoplegia: analysis of 86 patients