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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
Author(s) -
PARK H. J.,
SONG K. S.,
NAH B. M.,
CHOI J. R.,
KIM M. J.
Publication year - 2005
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.1538-7836.2005.01144.x
Subject(s) - purpura fulminans , exon , gene , genetics , base (topology) , biology , medicine , mathematics , dermatology , mathematical analysis