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

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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Veröffentlicht in:Indian journal of dermatology, venereology, and leprology venereology, and leprology, 2024-04, p.1-3, Article 1
Hauptverfasser: Francis, Aneeta, George, Anuja Elizabeth, Ashok, Priya, Chandran, Reena
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creator Francis, Aneeta
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Chandran, Reena
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doi_str_mv 10.25259/IJDVL_618_2023
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source Bioline International; EZB-FREE-00999 freely available EZB journals
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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