Totomoch-Serra, A., Marquez, M. F., & Cervantes-Barragán, D. E. (2017). Sanger sequencing as a first-line approach for molecular diagnosis of Andersen-Tawil syndrome [version 1; peer review: 3 approved]. F1000 research, 6, 1016. https://doi.org/10.12688/f1000research.11610.1
Chicago Style (17th ed.) CitationTotomoch-Serra, Armando, Manlio F. Marquez, and David E. Cervantes-Barragán. "Sanger Sequencing as a First-line Approach for Molecular Diagnosis of Andersen-Tawil Syndrome [version 1; Peer Review: 3 Approved]." F1000 Research 6 (2017): 1016. https://doi.org/10.12688/f1000research.11610.1.
MLA (9th ed.) CitationTotomoch-Serra, Armando, et al. "Sanger Sequencing as a First-line Approach for Molecular Diagnosis of Andersen-Tawil Syndrome [version 1; Peer Review: 3 Approved]." F1000 Research, vol. 6, 2017, p. 1016, https://doi.org/10.12688/f1000research.11610.1.