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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

✍ Scribed by K. K. ABU-AMERO; T. M. OWAIDAH; M. AL-MAHED

Book ID: 109151490
Publisher: John Wiley and Sons
Year: 2006
Tongue: English
Weight: 177 KB
Volume: 4
Category: Article
ISSN: 1538-7933
DOI: 10.1111/j.1538-7836.2006.01894.x

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