Identification and characterisation of mutations associated with von Willebrand disease in a Turkish patient cohort

Several cohort studies have investigated the molecular basis of von Willebrand disease (VWD); however these have mostly focused on European and North American populations. This study aimed to investigate mutation spectrum in 26 index cases (IC) from Turkey diagnosed with all three VWD types, the maj...

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Detalhes bibliográficos
Main Authors: Hampshire, Daniel J., Abuzenadah, Adel M., Cartwright, Ashley, Al-Shammari, Nawal S., Coyle, Rachael E., Eckert, Michaela, Al-Buhairan, Ahlam M., Messenger, Sarah L., Budde, Ulrich, Gürsel, Türkiz, Ingerslev, Jørgen, Peake, Ian R., Goodeve, Anne C.
Formato: Artigo
Idioma:Inglês
Publicado em: 2013
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4213552/
https://ncbi.nlm.nih.gov/pubmed/23702511
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1160/TH13-02-0135
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