APA (7th ed.) Citation

SL, C., C, S., L, K., N, V., D, O., L, H., . . . NP, S. (2024). SMN1 c.5C>G (p.Ala2Gly) missense variant, a challenging molecular SMA diagnosis associated with mild disease, preserves SMN nuclear gems in patient-specific fibroblasts. Frontiers in genetics, 15, 1406819. https://doi.org/10.3389/fgene.2024.1406819

Chicago Style (17th ed.) Citation

SL, Cook, et al. "SMN1 C.5C>G (p.Ala2Gly) Missense Variant, a Challenging Molecular SMA Diagnosis Associated with Mild Disease, Preserves SMN Nuclear Gems in Patient-specific Fibroblasts." Frontiers in Genetics 15 (2024): 1406819. https://doi.org/10.3389/fgene.2024.1406819.

MLA (9th ed.) Citation

SL, Cook, et al. "SMN1 C.5C>G (p.Ala2Gly) Missense Variant, a Challenging Molecular SMA Diagnosis Associated with Mild Disease, Preserves SMN Nuclear Gems in Patient-specific Fibroblasts." Frontiers in Genetics, vol. 15, 2024, p. 1406819, https://doi.org/10.3389/fgene.2024.1406819.