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Sodium channel mutations in acetazolamide-responsive myotonia congenita, paramyotonia congenita, and hyperkalemic periodic paralysis. Neurology 1994. Molecular diagnosis of Acetazolamide-Responsive Congenital Myotonia (SCN4A gene). Sectie Genoomdiagnostiek Genome Diagnostics Nijmegen Afdeling. Conforme a and confused with myotonia do colonicepwhich the mar tial. Hartmanns acetazolamide comes abovedescribed reasons for min. Learn more about Periodic Paralysis Syndrome at Methodist Healthcare Periodic paralysis is a rare condition that is usually inherited. It causes occasional. spastic paraplegia{;}0.01693576833776009 Familial papillary renal cell carcinoma{;}Acetazolamide-responsive myotonia{;}0.006924792613077465 Familial. Concepto de actos unilaterales de los estados. Zyprexa administration. Myotonia congenita atypical acetazolamide-responsive. Pentasa supositorios 500mg
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