Use of next-generation sequencing and candidate gene analysis to identify underlying defects in patients with inherited platelet function disorders

Leo, V.C., Morgan, N.V., Bem, D. et al. (9 more authors) (2015) Use of next-generation sequencing and candidate gene analysis to identify underlying defects in patients with inherited platelet function disorders. Journal of Thrombosis and Haemostasis, 13 (4). pp. 643-650. ISSN 1538-7933

Abstract

Metadata

Authors/Creators:
Copyright, Publisher and Additional Information: © 2014 The Authors. Journal of Thrombosis and Haemostasis published by Wiley Periodicals, Inc. on behalf of International Society on Thrombosis and Haemostasis. This is an open access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
Keywords: bioinformatics; bleeding; blood platelet disorders; high-throughput DNA sequencing; platelets
Dates:
  • Published: April 2015
  • Accepted: 14 December 2014
  • Published (online): 27 January 2015
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 > Sheffield Teaching Hospitals
Funding Information:
FunderGrant number
UNIVERSITY OF BIRMINGHAMRCS Ref 09-0919
Depositing User: Symplectic Sheffield
Date Deposited: 28 Oct 2016 15:14
Last Modified: 28 Oct 2016 15:14
Published Version: https://dx.doi.org/10.1111/jth.12836
Status: Published
Publisher: Wiley
Refereed: Yes
Identification Number: https://doi.org/10.1111/jth.12836

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