The human skeletal muscle Na channel mutation R669H associated with hypokalemic periodic paralysis enhances slow inactivation. (Q40907023)
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English | The human skeletal muscle Na channel mutation R669H associated with hypokalemic periodic paralysis enhances slow inactivation. |
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The human skeletal muscle Na channel mutation R669H associated with hypokalemic periodic paralysis enhances slow inactivation (English)
A F Struyk
K A Scoggan
D E Bulman
1 December 2000
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