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Article

Severe type I protein C deficiency with neonatal purpura fulminans due to a novel homozygous mutation in exon 6 of the protein C gene.

Journal of thrombosis and haemostasis : JTH - 1 May 2006

Abu-Amero K K, Owaidah T M, Al-Mahed M

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PMID: 16689776
DOI: 10.1111/j.1538-7836.2006.01894.x

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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Severe type I protein C deficiency with neonatal purpura fulminans due to a novel homozygous mutation in exon 6 of the protein C gene.PMID 16689776Read ↗

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