A New (K1518E) Candidate Mutation Detected by Universal Heteroduplex Generator Analysis in a Patient with Type 2A (Phenotype IIA) von Willebrand Disease - Enayat, Mohammad S.; Theophilus, Bimal D. M.; Hill, Frank G. H.; Rose, Peter E.; Culpan, Doris; Bidwell, Jeffery; Standen, Graham R. (Thrombosis and Haemostasis, 1998)