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Combined Deficiency of Vitamin K-Dependent Clotting Factors 1
A hereditary combined deficiency of vitamin K-dependent clotting factors that is caused by homozygous or compound heterozygous mutation in the GGCX gene on chromosome 2p11.2.
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Overview
A hereditary combined deficiency of vitamin K-dependent clotting factors that is caused by homozygous or compound heterozygous mutation in the GGCX gene on chromosome 2p11.2.
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