TY  - CONF

T1  - Missense mutations located in the von Willebrand factor (VWF) D1 domain cause quantitative VWF deficiency through impairment of VWF packaging into storage organelles

JO  - Journal of Thrombosis and Haemostasis

PY  - 2015/06/03

AU  - Dsouza MM

AU  - Webster SJ

AU  - McMaster J

AU  - Cartwright A

AU  - Budde U

AU  - Peake IR

AU  - Goodeve AC

AU  - Hampshire DJ

AU  - EU-VWD and ZPMCB-VWD study groups

ED  - 

DO  - DOI: 10.1111/jth.12993

PB  - Wiley

VL  - 13

IS  - Suppl. 2

SP  - 508

EP  - 508

Y2  - 2025/04/05

ER  -