A new (K1518E) candidate mutation detected by universal heteroduplex generator analysis in a patient with Type 2A (Phenotype IIA) von Willebrand's disease

MS Enayat, BDM Theophilus, FGH Hill, PE Rose, D Heinemann-Culpan, JL Bidwell, G Standen

Research output: Contribution to journalArticle (Academic Journal)

Translated title of the contributionA new (K1518E) candidate mutation detected by universal heteroduplex generator analysis in a patient with Type 2A (Phenotype IIA) von Willebrand's disease
Original languageEnglish
Pages (from-to)240
JournalThrombosis and Haemostasis
Volume79
Publication statusPublished - 1998

Cite this

Enayat, MS., Theophilus, BDM., Hill, FGH., Rose, PE., Heinemann-Culpan, D., Bidwell, JL., & Standen, G. (1998). A new (K1518E) candidate mutation detected by universal heteroduplex generator analysis in a patient with Type 2A (Phenotype IIA) von Willebrand's disease. Thrombosis and Haemostasis, 79, 240.