Yazar "Lillicrap, David" için listeleme
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Functional characterisation of the type 1 von Willebrand disease candidate VWF gene variants: p. M771I, p. L881R and p. P1413L
Berber, Ergül; Özbil, Mehmet; Brown, Christine; Başlar, Zafer; Çağlayan, S. Hande; Lillicrap, David (SIMTI Servizi, 2017)Background. Abnormalities in the biosynthetic pathway or increased clearance of plasma von Willebrand factor (VWF) are likely to contribute to decreased plasma VWF levels in inherited type 1 von Willebrand disease (VWD). ...
