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Article

A common VWF exon 28 haplotype in the Turkish population.

Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis - 1 Sept 2013

Berber Ergul, Pehlevan Funda, Akin Mehmet, Capan Ozlem Yalcin, Kavakli Kaan, Çaglayan S Hande

Abstract excerpt

An increasing number of mutations and polymorphisms have been identified in the von Willebrand factor (VWF) gene of patients with von Willebrand disease (VWD). Most of the sequence alterations are within exon 28, duplicated in the VWF pseudogene on chromosome 22. Genetic recombination causing the gene conversion between the VWF gene and its pseudogene is associated with multiple substitutions in the VWF gene and...

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PMID: 22473027
DOI: 10.1177/1076029612441054

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VWF

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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