Dysfibrinogenaemia associated with a novel heterozygous mutation in FGB (c.680delG) and a mild clinical history of bleeding.
| Data(s) |
01/03/2015
|
|---|---|
| Formato |
application/pdf |
| Identificador |
http://boris.unibe.ch/79767/1/Seiten_231_232_aus%2000001721-201503000-00021-2.pdf Priovolos, Anna; Neerman-Arbez, Marguerite; Morris, Michael; Angelillo, Anne; Noetzli, Jasmine Madeleine (2015). Dysfibrinogenaemia associated with a novel heterozygous mutation in FGB (c.680delG) and a mild clinical history of bleeding. Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis, 26(2), pp. 231-232. Lippincott Williams & Wilkins 10.1097/MBC.0000000000000196 <http://dx.doi.org/10.1097/MBC.0000000000000196> doi:10.7892/boris.79767 info:doi:10.1097/MBC.0000000000000196 info:pmid:25629419 urn:issn:0957-5235 |
| Idioma(s) |
eng |
| Publicador |
Lippincott Williams & Wilkins |
| Relação |
http://boris.unibe.ch/79767/ |
| Direitos |
info:eu-repo/semantics/openAccess |
| Fonte |
Priovolos, Anna; Neerman-Arbez, Marguerite; Morris, Michael; Angelillo, Anne; Noetzli, Jasmine Madeleine (2015). Dysfibrinogenaemia associated with a novel heterozygous mutation in FGB (c.680delG) and a mild clinical history of bleeding. Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis, 26(2), pp. 231-232. Lippincott Williams & Wilkins 10.1097/MBC.0000000000000196 <http://dx.doi.org/10.1097/MBC.0000000000000196> |
| Palavras-Chave | #610 Medicine & health |
| Tipo |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion PeerReviewed |
