Identification and characterisation of mutations associated with von Willebrand disease in a Turkish patient cohort
(2013)
Journal Article
Hampshire, D. J., Abuzenadah, A. M., Cartwright, A., Al-Shammari, N. S., Coyle, R. E., Eckert, M., Al-Buhairan, A. M., Messenger, S. L., Budde, U., Gürsel, T., Ingerslev, J., Peake, I. R., & Goodeve, A. C. (2013). Identification and characterisation of mutations associated with von Willebrand disease in a Turkish patient cohort. Thrombosis and haemostasis, 110(2), 264-274. https://doi.org/10.1160/TH13-02-0135
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... Read More about Identification and characterisation of mutations associated with von Willebrand disease in a Turkish patient cohort.