Struyk, A. F., Scoggan, K. A., Bulman, D. E., & Cannon, S. C. (2000). The Human Skeletal Muscle Na Channel Mutation R669H Associated with Hypokalemic Periodic Paralysis Enhances Slow Inactivation. J Neurosci.
Style de citation ChicagoStruyk, Arie F., Kylie A. Scoggan, Dennis E. Bulman, et Stephen C. Cannon. "The Human Skeletal Muscle Na Channel Mutation R669H Associated With Hypokalemic Periodic Paralysis Enhances Slow Inactivation." J Neurosci 2000.
Style de citation MLAStruyk, Arie F., Kylie A. Scoggan, Dennis E. Bulman, et Stephen C. Cannon. "The Human Skeletal Muscle Na Channel Mutation R669H Associated With Hypokalemic Periodic Paralysis Enhances Slow Inactivation." J Neurosci 2000.
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