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.; Hampshire, D. J.

Abstract

Letter to the editor

Citation

Cartwright, A., Peake, I. R., Goodeve, A. C., & Hampshire, D. J. (2016). In silico analysis highlights the copy number variation mechanism responsible for the historically reported VWF exon 42 deletion. Haemophilia, 22(5), e484-e487. https://doi.org/10.1111/hae.13059

• Journal Article Type: Letter
• Acceptance Date: Jul 2, 2016
• Online Publication Date: Aug 1, 2016
• Publication Date: Sep 21, 2016
• Deposit Date: Apr 10, 2019
• Journal: Haemophilia
• Print ISSN: 1351-8216
• Publisher: Wiley
• Peer Reviewed: Peer Reviewed
• Volume: 22
• Issue: 5
• Pages: e484-e487
• DOI: https://doi.org/10.1111/hae.13059
• Public URL: https://hull-repository.worktribe.com/output/1581246
• Publisher URL: https://onlinelibrary.wiley.com/doi/full/10.1111/hae.13059
• Related Public URLs: http://eprints.whiterose.ac.uk/103473/