The periodic paralysis(PP) are rare autosomal-dominant disorders associated to mutations in the skeletal muscle sodium. calcium and potassium channel genes characterized by muscle fiber depolarization with un-excitability. episodes of weakness with variations in serum potassium concentrations. Recent advances in thyrotoxic-PP(TPP) and hypokalemic-PP(hypoPP) confirm the involvement of ... https://herbsdailyes.shop/product-category/dl-phenylalanine/