APA (7th ed.) Citation

S, L., O, S., C, P., C, M., Y, H., M, R., . . . DA, T. (2020). A novel rare c.-39C>T mutation in the PROS1 5'UTR causing PS deficiency by creating a new upstream translation initiation codon. Clinical science (London, England : 1979), 134(10), 1181. https://doi.org/10.1042/CS20200403

Chicago Style (17th ed.) Citation

S, Labrouche-Colomer, et al. "A Novel Rare C.-39C>T Mutation in the PROS1 5'UTR Causing PS Deficiency by Creating a New Upstream Translation Initiation Codon." Clinical Science (London, England : 1979) 134, no. 10 (2020): 1181. https://doi.org/10.1042/CS20200403.

MLA (9th ed.) Citation

S, Labrouche-Colomer, et al. "A Novel Rare C.-39C>T Mutation in the PROS1 5'UTR Causing PS Deficiency by Creating a New Upstream Translation Initiation Codon." Clinical Science (London, England : 1979), vol. 134, no. 10, 2020, p. 1181, https://doi.org/10.1042/CS20200403.