Share
Other content recommended for you
- Genetic neurological channelopathies: molecular genetics and clinical phenotypes
- Skeletal muscle channelopathies: a guide to diagnosis and management
- Muscle disease
- Muscle hypertrophy and pseudohypertrophy
- Focal and abnormally persistent paralysis associated with congenital paramyotonia
- Investigating the genetic susceptibility to exertional heat illness
- Diagnosis and new treatment in muscle channelopathies
- Redefining the clinical phenotypes of non-dystrophic myotonic syndromes
- Dominantly inherited proximal myotonic myopathy and leukoencephalopathy in a family with an incidental CLCN1 mutation
- Neurological channelopathies