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Severe protein S deficiency resulting from two novel mutations in PROS1 presenting with a relatively mild clinical phenotype
Author(s) -
CARTER I. S. R.,
HEWITT J.,
PU C. H.,
WU J. K.,
CARTER C. J.,
MACGILLIVRAY R. T. A.
Publication year - 2008
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.1538-7836.2008.03012.x
Subject(s) - phenotype , clinical phenotype , medicine , protein s deficiency , mutation , protein s , genetics , biology , protein c , gene