Identification of a novel nonsense mutation leading to congenital factor XIII deficiency.

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)

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 and 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:

12 Dec 2019 05:12

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

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