Whole exome sequencing identifies genetic variants in inherited thrombocytopenia with secondary qualitative function defects

UK GAPP Study Group, Paul Harrison

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

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The functional role of ANKRD18A in megakaryocytes and platelets
Morgan, N. (Principal Investigator) & Watson, S. (Co-Investigator)
BRITISH HEART FOUNDATION
1/01/14 → 30/09/15
Project: Research
Molecular Genetic Investigation of Patients with Congenital Thrombocytopenias
Morgan, N. (Principal Investigator), Harrison, P. (Co-Investigator), Lowe, G. (Co-Investigator) & Watson, S. (Co-Investigator)
BRITISH HEART FOUNDATION
18/11/13 → 17/11/16
Project: Research