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Initial published Come july 1st One, 2009; doi:15.1152/ajpcell.00519.2008.-Andersen’s syndrome can be a rare condition that is identified using a triad: routine paralysis, heart failure arrhythmia, and development anomalies. Muscle tissue weakness has become described within two-thirds of the patients. KCNJ2 remains the merely gene connected to […] Виж
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