Cite
INF2 mutations in patients with a broad phenotypic spectrum of Charcot‐Marie‐Tooth disease and focal segmental glomerulosclerosis.
MLA
Park, Jin Hee, et al. “INF2 Mutations in Patients with a Broad Phenotypic Spectrum of Charcot‐Marie‐Tooth Disease and Focal Segmental Glomerulosclerosis.” Journal of the Peripheral Nervous System, vol. 28, no. 1, Mar. 2023, pp. 108–18. EBSCOhost, https://doi.org/10.1111/jns.12530.
APA
Park, J. H., Kwon, H. M., Nam, D. E., Kim, H. J., Nam, S. H., Kim, S. B., Choi, B., & Chung, K. W. (2023). INF2 mutations in patients with a broad phenotypic spectrum of Charcot‐Marie‐Tooth disease and focal segmental glomerulosclerosis. Journal of the Peripheral Nervous System, 28(1), 108–118. https://doi.org/10.1111/jns.12530
Chicago
Park, Jin Hee, Hye Mi Kwon, Da Eun Nam, Hye Jin Kim, Soo Hyun Nam, Sang Beom Kim, Byung‐Ok Choi, and Ki Wha Chung. 2023. “INF2 Mutations in Patients with a Broad Phenotypic Spectrum of Charcot‐Marie‐Tooth Disease and Focal Segmental Glomerulosclerosis.” Journal of the Peripheral Nervous System 28 (1): 108–18. doi:10.1111/jns.12530.