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.
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| Title: | 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. |
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| Authors: | Francis, Aneeta1 (AUTHOR) aneetagreek@gmail.com, George, Anuja Elizabeth1 (AUTHOR), Ashok, Priya1 (AUTHOR), Chandran, Reena1 (AUTHOR) |
| Source: | Indian Journal of Dermatology, Venereology & Leprology. 2025 Supplement, Vol. 91, p1-3. 3p. |
| Database: | Academic Search Ultimate |
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| ISSN: | 03786323 |
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| DOI: | 10.25259/IJDVL_618_2023 |
