Enrichment of FLI1 and RUNX1 mutations in families with excessive bleeding and platelet dense granule secretion defects

J. Stockley, N. V. Morgan, D. Bem, G. C. Lowe, M. Lordkipanidze, B. Dawood, M. A. Simpson, K. Macfarlane, K. Horner, V. C. Leo, K. Talks, J. Motwani, J. T. Wilde, P. W. Collins, M. Makris, S. P. Watson, M. E. Daly

Research output: Contribution to journal › Article › peer-review

81 Citations (Scopus)

778 Downloads (Pure)

4 results

Finished
Molecular Genetic Investigation of Patients with Congenital Thrombocytopenias
Morgan, N., Harrison, P., Lowe, G. & Watson, S.
British Heart Foundation
18/11/13 → 17/11/16
Project: Research
Do Patients who Exhibit Serious Bleeds on Anti-Platelet Therapy have a Previously Undiagnosed Defect in Platelet Function
Watson, S.
British Heart Foundation
1/06/11 → 31/05/13
Project: Research
Phenotyping and Genotyping of Platelet Defects in Patient Populations Enriched in Bleeding
Watson, S.
THE WELLCOME TRUST
4/10/10 → 3/10/13
Project: Research
Mapping and Functional Investigation of Genetic Mutations in Patients with Mild, Platelet Bleeding Disorders
Watson, S.
British Heart Foundation
1/02/10 → 31/01/15
Project: Research