Kim, H. J., Hong, Y. B., Park, J., Choi, Y., Kim, Y. J., Yoon, B. R., . . . Choi, B. (2013). Mutations in the PLEKHG5 gene is relevant with autosomal recessive intermediate Charcot-Marie-Tooth disease. Orphanet Journal of Rare Diseases, 8(1), 1. https://doi.org/10.1186/1750-1172-8-104
Chicago Style (17th ed.) CitationKim, Hyeon Jin, et al. "Mutations in the PLEKHG5 Gene Is Relevant with Autosomal Recessive Intermediate Charcot-Marie-Tooth Disease." Orphanet Journal of Rare Diseases 8, no. 1 (2013): 1. https://doi.org/10.1186/1750-1172-8-104.
MLA (9th ed.) CitationKim, Hyeon Jin, et al. "Mutations in the PLEKHG5 Gene Is Relevant with Autosomal Recessive Intermediate Charcot-Marie-Tooth Disease." Orphanet Journal of Rare Diseases, vol. 8, no. 1, 2013, p. 1, https://doi.org/10.1186/1750-1172-8-104.