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.
استشهاد بنمط شيكاغوStruyk, Arie F., Kylie A. Scoggan, Dennis E. Bulman, و Stephen C. Cannon. "The Human Skeletal Muscle Na Channel Mutation R669H Associated With Hypokalemic Periodic Paralysis Enhances Slow Inactivation." J Neurosci 2000.
MLA استشهادStruyk, Arie F., Kylie A. Scoggan, Dennis E. Bulman, و Stephen C. Cannon. "The Human Skeletal Muscle Na Channel Mutation R669H Associated With Hypokalemic Periodic Paralysis Enhances Slow Inactivation." J Neurosci 2000.
تحذير: قد لا تكون هذه الاستشهادات دائما دقيقة بنسبة 100%.