APA (7th ed.) Citation

Lee, Y. J., Kim, S. Y., Kim, M. J., Kim, A. R., Lee, J., & Chae, J. (2021). Infant with early onset bilateral facial and bulbar weakness: Successful treatment of riboflavin in multiple acyl-CoA dehydrogenase deficiency caused by biallelic nonsense FLAD1 variants. Neuromuscular Disorders, 31(11), 1194. https://doi.org/10.1016/j.nmd.2021.07.006

Chicago Style (17th ed.) Citation

Lee, Yun Jeong, Soo Yeon Kim, Man Jin Kim, Ae Ryoung Kim, Jong-Mok Lee, and Jong-Hee Chae. "Infant with Early Onset Bilateral Facial and Bulbar Weakness: Successful Treatment of Riboflavin in Multiple Acyl-CoA Dehydrogenase Deficiency Caused by Biallelic Nonsense FLAD1 Variants." Neuromuscular Disorders 31, no. 11 (2021): 1194. https://doi.org/10.1016/j.nmd.2021.07.006.

MLA (9th ed.) Citation

Lee, Yun Jeong, et al. "Infant with Early Onset Bilateral Facial and Bulbar Weakness: Successful Treatment of Riboflavin in Multiple Acyl-CoA Dehydrogenase Deficiency Caused by Biallelic Nonsense FLAD1 Variants." Neuromuscular Disorders, vol. 31, no. 11, 2021, p. 1194, https://doi.org/10.1016/j.nmd.2021.07.006.