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Novel phenotype and γ-glutamyl carboxylase mutations in combined deficiency of vitamin K-dependent coagulation factors.

Haemophilia : the official journal of the World Federation of Hemophilia - 1 Sept 2011

Lunghi B, Redaelli R, Caimi T M, Corno A R, Bernardi F, Marchetti G

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PMID: 21435120
DOI: 10.1111/j.1365-2516.2011.02524.x

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