APA (7th ed.) Citation

N, S., EB, F., D, O., SA, L., & B, L. (2020). X-linked infantile spinal muscular atrophy (SMAX2) caused by novel c.1681G>A substitution in the UBA1 gene, expanding the phenotype. Neuromuscular disorders : NMD, 30(1), 35. https://doi.org/10.1016/j.nmd.2019.11.004

Chicago Style (17th ed.) Citation

N, Shaughnessy, Forman EB, O'Rourke D, Lynch SA, and Lynch B. "X-linked Infantile Spinal Muscular Atrophy (SMAX2) Caused by Novel C.1681G>A Substitution in the UBA1 Gene, Expanding the Phenotype." Neuromuscular Disorders : NMD 30, no. 1 (2020): 35. https://doi.org/10.1016/j.nmd.2019.11.004.

MLA (9th ed.) Citation

N, Shaughnessy, et al. "X-linked Infantile Spinal Muscular Atrophy (SMAX2) Caused by Novel C.1681G>A Substitution in the UBA1 Gene, Expanding the Phenotype." Neuromuscular Disorders : NMD, vol. 30, no. 1, 2020, p. 35, https://doi.org/10.1016/j.nmd.2019.11.004.