DOI: 10.1055/s-00000077

Seminars in Thrombosis and Hemostasis

Referenz

Casini A, Brungs T, Lavenu-Bombled C, Vilar R, Neerman-Arbez M, de Moerloose P.
Genetics, diagnosis and clinical features of congenital hypodysfibrinogenemia: a systematic literature review and report of a novel mutation.

J Thromb Haemost 2017;
15 (05) 876-888

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