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Classification of exon 18 linked variants of VWF gene in von Willebrand disease

Defects in von Willebrand factor, a crucial protein in haemostasis, lead to the most common inherited coagulopathy in man, von Willebrand disease. To date, over 350 mutations and 170 single nucleotide polymorphisms of VWF gene have been reported. In the present study, the distribution of two linked...

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Detalhes bibliográficos
Main Authors: Shahbazi, Shirin, Alavi, Sara, Mahdian, Reza
Formato: Artigo
Idioma:Inglês
Publicado em: e-Century Publishing Corporation 2012
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3316446/
https://ncbi.nlm.nih.gov/pubmed/22493754
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