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VITAMIN K-DEPENDENT CLOTTING FACTORS, COMBINED DEFICIENCY OF, 1
Known as:
Familial Multiple Coagulation Factor Deficiency III
, VKCFD1
, VKCFD
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National Institutes of Health
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Related topics
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2 relations
Broader (1)
Blood Coagulation Disorders, Inherited
GGCX gene
Papers overview
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2008
2008
Recombinant expression of wildtype and mutated γ-glutamyl carboxylase
K. Siegel
,
S. Rost
,
C. Mueller
,
J. Oldenburg
Hämostaseologie
2008
Corpus ID: 71024928
So far, only 10 different mutations have been identified in the GGCX gene of VKCFD patients. Four of them (Trp157Arg, Leu394Arg…
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