Burley, KateWhyte, Claire S.Westbury, Sarah K.Walker, MaryStirrups, Kathleen ETurro, ErnestChapman, OliverReilly-Stitt, ChristopherMutch, Nicola J.Mumford, Andrew D.2017-07-192017-07-192016-10-06Burley, K, Whyte, C S, Westbury, S K, Walker, M, Stirrups, K E, Turro, E, Chapman, O, Reilly-Stitt, C, Mutch, N J & Mumford, A D 2016, 'Altered fibrinolysis in autosomal dominant thrombomodulin-associated coagulopathy', Blood, vol. 128, no. 14, pp. 1879-1883. https://doi.org/10.1182/blood-2016-05-7160920006-4971ORCID: /0000-0001-8127-6102/work/101050686ORCID: /0000-0002-7452-0813/work/169538882http://hdl.handle.net/2164/8972The NIHR BioResource-Rare Diseases and the ThromboGenomics sequencing projects are supported by the National Institute for Health Research (NIHR; http://www.nihr.ac.uk). KB is an NIHR academic clinical fellow. SKW is supported by a Medical Research Council (MRC) Clinical Training Fellowship (MR/K023489/1). KS and ET are supported by the NIHR BioResource Rare Diseases. CSW and NJM are supported by the British Heart Foundation (FS/11/2/28579). ADM is supported by the NIHR Bristol Cardiovascular Biomedical Research Unit. Deposited in EuropePMC. PMCID:PMC505469951485737engR MedicineMedical Research Council (MRC)MR/K023489/1British Heart FoundationFS/11/2/28579National Institute for Health Research (NIHR)RJournal article10.1182/blood-2016-05-716092http://europepmc.org/abstract/MED/2743685112814