APA (7th ed.) Citation

Schätzl, T., Kaiser, L., & Deigner, H. (2021). Facioscapulohumeral muscular dystrophy: Genetics, gene activation and downstream signalling with regard to recent therapeutic approaches: an update. Orphanet Journal of Rare Diseases, 16(1), 1. https://doi.org/10.1186/s13023-021-01760-1

Chicago Style (17th ed.) Citation

Schätzl, Teresa, Lars Kaiser, and Hans-Peter Deigner. "Facioscapulohumeral Muscular Dystrophy: Genetics, Gene Activation and Downstream Signalling with Regard to Recent Therapeutic Approaches: An Update." Orphanet Journal of Rare Diseases 16, no. 1 (2021): 1. https://doi.org/10.1186/s13023-021-01760-1.

MLA (9th ed.) Citation

Schätzl, Teresa, et al. "Facioscapulohumeral Muscular Dystrophy: Genetics, Gene Activation and Downstream Signalling with Regard to Recent Therapeutic Approaches: An Update." Orphanet Journal of Rare Diseases, vol. 16, no. 1, 2021, p. 1, https://doi.org/10.1186/s13023-021-01760-1.