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Items for "CSGE"

Mutations in coagulation factor XIII A gene in eight unrelated Indians. Five novel mutations identified by a novel PCR-CSGE approach

Factor XIII deficiency is a rare autosomal (1:2,000,000) recessive disorder of blood coagulation usually attributed to mutations in the coagulation factor XIII (FXIII) A gene...

Keywords: factor XIII, mutation, CSGE

03/2006 | Thrombosis and Haemostasis, Schattauer