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

Report

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

Journal of thrombosis and haemostasis : JTH, Vol.4(5), pp.1152-1153

01/05/2006

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Title: Severe type I protein C deficiency with neonatal purpura fulminans due to a novel homozygous mutation in exon 6 of the protein C gene
Creators - without role: K K Abu-Amero
T M Owaidah
M Al-Mahed
Publication Details: Journal of thrombosis and haemostasis : JTH, Vol.4(5), pp.1152-1153
Identifiers: 9913889308331
Academic Unit: King Faisal University; Alfaisal University
Language: English
Resource Type: Report