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. - Francis, Aneeta; George, Anuja Elizabeth; Ashok, Priya; Chandran, Reena (Indian Journal of Dermatology, Venereology & Leprology, 2025)