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Article

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

Haemophilia : the official journal of the World Federation of Hemophilia - 1 Sept 2016

Cartwright A, Peake I R, Goodeve A C, Hampshire D J

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Topics

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Share to Base Sequence
Share to DNA Copy Number Variations
Share to Exons
Share to Molecular Sequence Data

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Polymorphism, Single Nucleotide

Share to Sequence Alignment

Share to Sequence Deletion

Share to von Willebrand Factor

Source

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Identifiers

PMID: 27481636
DOI: 10.1111/hae.13059
PMCID: PMC5960579

Genes

VWF

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

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