Li, Bojun; Borhany, Munira; Abid, Madiha; Kohler, Hans-Peter; Schroeder, Verena (2018). Identification of a novel nonsense mutation leading to congenital factor XIII deficiency. Thrombosis research, 165, pp. 83-85. Elsevier 10.1016/j.thromres.2018.03.019
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Item Type: |
Journal Article (Further Contribution) |
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Division/Institute: |
04 Faculty of Medicine > Pre-clinic Human Medicine > BioMedical Research (DBMR) > Forschungsbereich Pavillon 52 > Forschungsgruppe Experimentelle Hämostase 04 Faculty of Medicine > Pre-clinic Human Medicine > BioMedical Research (DBMR) |
UniBE Contributor: |
Li, Bojun, Kohler, Hans-Peter, Schröder, Verena |
Subjects: |
600 Technology > 610 Medicine & health |
ISSN: |
0049-3848 |
Publisher: |
Elsevier |
Language: |
English |
Submitter: |
Marla Rittiner |
Date Deposited: |
23 Jan 2019 15:09 |
Last Modified: |
05 Dec 2022 15:23 |
Publisher DOI: |
10.1016/j.thromres.2018.03.019 |
PubMed ID: |
29604433 |
Uncontrolled Keywords: |
Congenital factor XIII deficiency Cys327Stop F13A gene mutations Factor XIII Rare bleedings disorders |
BORIS DOI: |
10.7892/boris.122564 |
URI: |
https://boris.unibe.ch/id/eprint/122564 |