Identification and characterisation of mutations associated with von Willebrand disease in a Turkish patient cohort

Hampshire, D.J. orcid.org/0000-0002-1387-8926, Abuzenadah, A.M., Cartwright, A. et al. (10 more authors) (2013) Identification and characterisation of mutations associated with von Willebrand disease in a Turkish patient cohort. Thrombosis and Haemostasis, 110 (2). pp. 264-274. ISSN 0340-6245

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Copyright, Publisher and Additional Information: © 2013 Schattauer. This is an author produced version of a paper subsequently published in Thrombosis and Haemostasis. Uploaded in accordance with the publisher's self-archiving policy.
Keywords: von Willebrand disease; mutation analysis; Large-scale deletion; multiplex ligation-dependent probe amplification; recessive 2A
Dates:
  • Published: August 2013
  • Published (online): 23 May 2013
  • Accepted: 4 May 2013
Institution: The University of Sheffield
Academic Units: The University of Sheffield > Faculty of Medicine, Dentistry and Health (Sheffield) > Department of Cardiovascular Science (Sheffield)
The University of Sheffield > Faculty of Medicine, Dentistry and Health (Sheffield) > School of Medicine (Sheffield) > Division of Genomic Medicine (Sheffield) > Department of Oncology (Sheffield)
The University of Sheffield > Sheffield Teaching Hospitals
Depositing User: Symplectic Sheffield
Date Deposited: 01 Mar 2017 13:03
Last Modified: 23 Mar 2018 08:39
Published Version: https://doi.org/10.1160/TH13-02-0135
Status: Published
Publisher: Schattauer
Refereed: Yes
Identification Number: https://doi.org/10.1160/TH13-02-0135
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