Dysfibrinogenaemia associated with a novel heterozygous mutation in FGB (c.680delG) and a mild clinical history of bleeding.

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

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Item Type:

Journal Article (Further Contribution)

Division/Institute:

04 Faculty of Medicine > Department of Haematology, Oncology, Infectious Diseases, Laboratory Medicine and Hospital Pharmacy (DOLS) > Clinic of Haematology and Central Haematological Laboratory
04 Faculty of Medicine > Pre-clinic Human Medicine > BioMedical Research (DBMR) > Unit Childrens Hospital > Forschungsgruppe Hämatologie (Erwachsene)

UniBE Contributor:

Angelillo, Anne and Noetzli, Jasmine Madeleine

Subjects:

600 Technology > 610 Medicine & health

ISSN:

0957-5235

Publisher:

Lippincott Williams & Wilkins

Language:

English

Submitter:

Verena Zwahlen

Date Deposited:

24 Mar 2016 11:13

Last Modified:

12 Sep 2017 15:16

Publisher DOI:

10.1097/MBC.0000000000000196

PubMed ID:

25629419

BORIS DOI:

10.7892/boris.79767

URI:

https://boris.unibe.ch/id/eprint/79767

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