In silico analysis highlights the copy number variation mechanism responsible for the historically reported VWF exon 42 deletion.

Cartwright, A., Peake, I.R., Goodeve, A.C. et al. (1 more author) (2016) In silico analysis highlights the copy number variation mechanism responsible for the historically reported VWF exon 42 deletion. Haemophilia. ISSN 1351-8216

Metadata

Authors/Creators:
  • Cartwright, A.
  • Peake, I.R.
  • Goodeve, A.C.
  • Hampshire, D.J.
Copyright, Publisher and Additional Information: © 2016 Wiley. This is an author produced version of a paper subsequently published in Haemophilia. Uploaded in accordance with the publisher's self-archiving policy.
Dates:
  • Published: 1 August 2016
  • Accepted: 2 July 2016
  • Published (online): 1 August 2016
Institution: The University of Sheffield
Academic Units: The University of Sheffield > Faculty of Medicine, Dentistry and Health (Sheffield) > School of Medicine (Sheffield)
Funding Information:
FunderGrant number
NATIONAL INSTITUTE OF HEALTH - UNITED STATES OF AMERICA2P01HL081588-06
Depositing User: Symplectic Sheffield
Date Deposited: 08 Aug 2016 10:18
Last Modified: 05 Aug 2017 13:40
Published Version: http://dx.doi.org/10.1111/hae.13059
Status: Published
Publisher: Wiley
Refereed: Yes
Identification Number: https://doi.org/10.1111/hae.13059
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