APA (7th ed.) Citation

Francis, A., George, A. E., Ashok, P., & Chandran, R. (2025). A novel homozygous missense mutation in exon 3 at codon 42 c.125G>A (p.Arg42His) in the PROC gene causing protein C deficiency and presenting as neonatal purpura fulminans. Indian Journal of Dermatology, Venereology & Leprology, 91, 1. https://doi.org/10.25259/IJDVL_618_2023

Chicago Style (17th ed.) Citation

Francis, Aneeta, Anuja Elizabeth George, Priya Ashok, and Reena Chandran. "A Novel Homozygous Missense Mutation in Exon 3 at Codon 42 C.125G>A (p.Arg42His) in the PROC Gene Causing Protein C Deficiency and Presenting as Neonatal Purpura Fulminans." Indian Journal of Dermatology, Venereology & Leprology 91 (2025): 1. https://doi.org/10.25259/IJDVL_618_2023.

MLA (9th ed.) Citation

Francis, Aneeta, et al. "A Novel Homozygous Missense Mutation in Exon 3 at Codon 42 C.125G>A (p.Arg42His) in the PROC Gene Causing Protein C Deficiency and Presenting as Neonatal Purpura Fulminans." Indian Journal of Dermatology, Venereology & Leprology, vol. 91, 2025, p. 1, https://doi.org/10.25259/IJDVL_618_2023.