DOI:
10.1055/s-00000077
Seminars in Thrombosis and Hemostasis
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References
Schroeder V, Meili E, Cung T, Schmutz P, Kohler HP.
Characterisation of six novel A-subunit mutations leading to congenital factor XIII deficiency and molecular analysis of the first diagnosed patient with this rare bleeding disorder.
Thromb Haemost 2006;
95 (1) 77-84
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