Identification of two novel missense mutations causing severe factor XIII deficiency.

Handrková, Helena; Borhany, M; Schroeder, Verena; Fatima, N; Hussain, A; Shamsi, T; Kohler, H P (2015). Identification of two novel missense mutations causing severe factor XIII deficiency. Haemophilia, 21(3), e253-e256. Blackwell Science 10.1111/hae.12663

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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 > 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 > Thromboselabor Kinderklinik [discontinued]

UniBE Contributor:

Handrková, Helena and Schröder, Verena

Subjects:

600 Technology > 610 Medicine & health

ISSN:

1351-8216

Publisher:

Blackwell Science

Language:

English

Submitter:

Verena Zwahlen

Date Deposited:

02 May 2016 11:26

Last Modified:

10 Dec 2019 14:43

Publisher DOI:

10.1111/hae.12663

PubMed ID:

25832324

BORIS DOI:

10.7892/boris.81595

URI:

https://boris.unibe.ch/id/eprint/81595

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