Dysfibrinogenaemia associated with a novel heterozygous mutation in FGB (c.680delG) and a mild clinical history of bleeding.
| Data(s) |
2015
|
|---|---|
| Identificador |
http://serval.unil.ch/?id=serval:BIB_822D5551B04F isbn:1473-5733 (Electronic) pmid:25629419 doi:10.1097/MBC.0000000000000196 isiid:000349007300021 |
| Idioma(s) |
en |
| Fonte |
Blood Coagulation and Fibrinolysis, vol. 26, no. 2, pp. 231-232 |
| Tipo |
info:eu-repo/semantics/article article |
