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
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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. | ||||
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Institution: | The University of Sheffield | ||||
Academic Units: | The University of Sheffield > Faculty of Medicine, Dentistry and Health (Sheffield) > The Medical School (Sheffield) | ||||
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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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