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

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Bibliographic Details
Published in:	Haemophilia : the official journal of the World Federation of Hemophilia Vol. 22; no. 5; pp. e484 - e487
Main Authors:	Cartwright, A., Peake, I. R., Goodeve, A. C., Hampshire, D. J.
Format:	Journal Article
Language:	English
Published:	England Blackwell Publishing Ltd 01-09-2016
Subjects:	Base Sequence DNA Copy Number Variations Exons Humans Molecular Sequence Data Polymorphism, Single Nucleotide Sequence Alignment Sequence Deletion von Willebrand Factor - genetics
Online Access:	Get full text
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Description
Bibliography:	UK Medical Research Council National Institutes of Health - No. HL081588 ArticleID:HAE13059 istex:462E7022845695A7BF2F2A286B3EC19A9E2AF775 ark:/67375/WNG-N7H7LNLD-P
ISSN:	1351-8216 1365-2516
DOI:	10.1111/hae.13059