Zhou, H., Jungbluth, H., Sewry, C. A., Feng, L., Bertini, E., Bushby, K., . . . Brown, S. (2007). Molecular mechanisms and phenotypic variation in RYR1-related congenital myopathies. Brain: A Journal of Neurology, 130(8), 2024. https://doi.org/10.1093/brain/awm096
Chicago Style (17th ed.) CitationZhou, Haiyan, et al. "Molecular Mechanisms and Phenotypic Variation in RYR1-related Congenital Myopathies." Brain: A Journal of Neurology 130, no. 8 (2007): 2024. https://doi.org/10.1093/brain/awm096.
MLA (9th ed.) CitationZhou, Haiyan, et al. "Molecular Mechanisms and Phenotypic Variation in RYR1-related Congenital Myopathies." Brain: A Journal of Neurology, vol. 130, no. 8, 2007, p. 2024, https://doi.org/10.1093/brain/awm096.
Warning: These citations may not always be 100% accurate.