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
![[img]](https://boris.unibe.ch/style/images/fileicons/text.png) |
Text
V.Schroeder_H.Handrkova_hae12663.pdf - Published Version Restricted to registered users only Available under License Publisher holds Copyright. Download (600kB) |
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: |
Röss, Helena, 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: |
02 Mar 2023 23:27 |
Publisher DOI: |
10.1111/hae.12663 |
PubMed ID: |
25832324 |
BORIS DOI: |
10.7892/boris.81595 |
URI: |
https://boris.unibe.ch/id/eprint/81595 |
Actions (login required)
 |
Edit item |