A, L., F, W., S, L., M, I., & TF, C. (2023). Skeletal muscle cell protein dysregulation highlights the pathogenesis mechanism of myopathy-associated p97/VCP R155H mutations. Frontiers in neurology, 14, 1211635. https://doi.org/10.3389/fneur.2023.1211635
Chicago Style (17th ed.) CitationA, Luzzi, Wang F, Li S, Iacovino M, and Chou TF. "Skeletal Muscle Cell Protein Dysregulation Highlights the Pathogenesis Mechanism of Myopathy-associated P97/VCP R155H Mutations." Frontiers in Neurology 14 (2023): 1211635. https://doi.org/10.3389/fneur.2023.1211635.
MLA (9th ed.) CitationA, Luzzi, et al. "Skeletal Muscle Cell Protein Dysregulation Highlights the Pathogenesis Mechanism of Myopathy-associated P97/VCP R155H Mutations." Frontiers in Neurology, vol. 14, 2023, p. 1211635, https://doi.org/10.3389/fneur.2023.1211635.