Homozygous type I Protein C deficiency in neonatal purpura fulminans with a novel frame-shift deletion of 10 base pairs in exon 8 of PROC gene. [electronic resource]

By: Contributor(s): Producer: 20050830Description: 593-5 p. digitalISSN:
  • 1538-7933
Subject(s): Online resources: In: Journal of thrombosis and haemostasis : JTH vol. 3
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Publication Type: Case Reports; Letter

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