Recent advances in the pathogenesis and drug actions in periodic paralyses and related channelophaties
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. Recen...
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| Main Authors: | , |
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| Format: | Book |
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Frontiers Media S.A.,
2011-02-01T00:00:00Z.
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