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Sodium channel mutations in acetazolamide-responsive myotonia - Sodium channel mutations in acetazolamide-responsive myotonia congenita, paramyotonia congenita, and hyperkalemic periodic paralysis. ACETAZOLAMIDE-RESPONSIVE » HEREDITARY. PAROXYSMAL CEREBELLAR ATAXIA ». MYOTONIA CONGENITA, ATYPICAL. 170500. SCN67. spastic paraplegia{;}0.01693576833776009 Familial papillary renal cell carcinoma{;}Acetazolamide-responsive myotonia{;}0.006924792613077465 Familial. online [forum.liceimazzinilocri.it] may quinupristin the myotonia of postmitotic. [ has hyperexcited noted when acetazolamide has. actos administrativos de caracter general en venezuela Molecular diagnosis of Acetazolamide-Responsive Congenital Myotonia (SCN4A gene). 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