APA (7th ed.) Citation

R, I., M, N., M, T., S, A., Y, Y., A, H., . . . H, M. (2023). Case report: Mitochondrial trifunctional protein deficiency caused by HADHB gene mutation (c.1175C>T) characterized by higher brain dysfunction followed by neuropathy, presented gadolinium enhancement on brain imaging in an adult patient. Frontiers in neurology, 14, 1187822. https://doi.org/10.3389/fneur.2023.1187822

Chicago Style (17th ed.) Citation

R, Ishikawa, Nakamori M, Takenaka M, Aoki S, Yamazaki Y, Hashiguchi A, Takashima H, and Maruyama H. "Case Report: Mitochondrial Trifunctional Protein Deficiency Caused by HADHB Gene Mutation (c.1175C>T) Characterized by Higher Brain Dysfunction Followed by Neuropathy, Presented Gadolinium Enhancement on Brain Imaging in an Adult Patient." Frontiers in Neurology 14 (2023): 1187822. https://doi.org/10.3389/fneur.2023.1187822.

MLA (9th ed.) Citation

R, Ishikawa, et al. "Case Report: Mitochondrial Trifunctional Protein Deficiency Caused by HADHB Gene Mutation (c.1175C>T) Characterized by Higher Brain Dysfunction Followed by Neuropathy, Presented Gadolinium Enhancement on Brain Imaging in an Adult Patient." Frontiers in Neurology, vol. 14, 2023, p. 1187822, https://doi.org/10.3389/fneur.2023.1187822.