PY, L., CT, H., HW, H., YJ, W., SJ, F., & YC, L. (2026). Intrafamilial Phenotypic Variation in Taiwanese Patients with Hereditary Spastic Paraplegia and Charcot-Marie-Tooth Disease Due to KIF5A Mutations: A Cross-Sectional Observational Study. Acta neurologica Taiwanica, 35(1), 30. https://doi.org/10.4103/ant.ANT-D-25-00042
Chicago Style (17th ed.) CitationPY, Lin, Hsiao CT, Huang HW, Wu YJ, Fu SJ, and Lee YC. "Intrafamilial Phenotypic Variation in Taiwanese Patients with Hereditary Spastic Paraplegia and Charcot-Marie-Tooth Disease Due to KIF5A Mutations: A Cross-Sectional Observational Study." Acta Neurologica Taiwanica 35, no. 1 (2026): 30. https://doi.org/10.4103/ant.ANT-D-25-00042.
MLA (9th ed.) CitationPY, Lin, et al. "Intrafamilial Phenotypic Variation in Taiwanese Patients with Hereditary Spastic Paraplegia and Charcot-Marie-Tooth Disease Due to KIF5A Mutations: A Cross-Sectional Observational Study." Acta Neurologica Taiwanica, vol. 35, no. 1, 2026, p. 30, https://doi.org/10.4103/ant.ANT-D-25-00042.