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Novel phenotype and γ‐glutamyl carboxylase mutations in combined deficiency of vitamin K‐dependent coagulation factors
Author(s) -
LUNGHI B.,
REDAELLI R.,
CAIMI T. M.,
CORNO A. R.,
BERNARDI F.,
MARCHETTI G.
Publication year - 2011
Publication title -
haemophilia
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.213
H-Index - 92
eISSN - 1365-2516
pISSN - 1351-8216
DOI - 10.1111/j.1365-2516.2011.02524.x
Subject(s) - hemostasis , medicine , hematology , vitamin k epoxide reductase , cyp2c9 , cytochrome p450 , metabolism