1. Use of next‐generation sequencing and candidate gene analysis to identify underlying defects in patients with inherited platelet function disorders. (27th January 2015) Authors: Leo, V. C.; Morgan, N. V.; Bem, D.; Jones, M. L.; Lowe, G. C.; Lordkipanidzé, M.; Drake, S.; Simpson, M. A.; Gissen, P.; Mumford, A.; Watson, S. P.; Daly, M. E.; the UK GAPP Study Group Journal: Journal of thrombosis and haemostasis Issue: Volume 13:Number 4(2015:Apr.) Page Start: 643 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗