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Mutations in either the essential or regulatory light chains of myosin are associated with a rare myopathy in human heart and skeletal muscle

Mitochondrial MyopathyCardiac MuscleCardiomyopathyMolecular PhysiologyRegulatory Light ChainsSkeletal MuscleGeneticsPhysiologyMolecular GeneticsCytoskeletonRare MyopathyMedicineCardiovascular GeneticsCardiac Pathology