Fan, C., Mao, N., Lehmann‐Horn, F., Bürmann, J., & Jurkat‐Rott, K. (2017). Effects of S906T polymorphism on the severity of a novel borderline mutation I692M in Na v1.4 cause periodic paralysis. Clinical Genetics, 91(6), 859. https://doi.org/10.1111/cge.12880
Chicago Style (17th ed.) CitationFan, C., N. Mao, F. Lehmann‐Horn, J. Bürmann, and K. Jurkat‐Rott. "Effects of S906T Polymorphism on the Severity of a Novel Borderline Mutation I692M in Na V1.4 Cause Periodic Paralysis." Clinical Genetics 91, no. 6 (2017): 859. https://doi.org/10.1111/cge.12880.
MLA (9th ed.) CitationFan, C., et al. "Effects of S906T Polymorphism on the Severity of a Novel Borderline Mutation I692M in Na V1.4 Cause Periodic Paralysis." Clinical Genetics, vol. 91, no. 6, 2017, p. 859, https://doi.org/10.1111/cge.12880.