Mutation spectrum and health status in skeletal muscle channelopathies in Japan
Ryogen Sasaki, Maki Nakaza, Mitsuru Furuta, Haruo Fujino, Tomoya Kubota, Masanori Takahashi
Topics & Concepts
Periodic paralysisPedigree chartMyotoniaHypokalemic periodic paralysisMyotonia congenitaSkeletal muscleMedicineParalysisEtiologyGeneticsChannelopathyMuscular dystrophyMuscle disorderMutationPediatricsMyotonic dystrophyInternal medicineBiologyGeneSurgeryIon channel regulation and functionCardiac electrophysiology and arrhythmiasGenetic Neurodegenerative Diseases