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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
Author(s) -
ABUAMERO K. K.,
OWAIDAH T. M.,
ALMAHED M.
Publication year - 2006
Publication title -
journal of thrombosis and haemostasis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.947
H-Index - 178
eISSN - 1538-7836
pISSN - 1538-7933
DOI - 10.1111/j.1538-7836.2006.01894.x
Subject(s) - purpura fulminans , medicine , protein c , protein c deficiency , disseminated intravascular coagulation , exon , coagulation , protein s , immunology , thrombosis , gene , biology , surgery , venous thrombosis , biochemistry