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Altered fibrinolysis in autosomal dominant thrombomodulin-associated coagulopathy

dc.contributor.authorBurley, Kate
dc.contributor.authorWhyte, Claire S.
dc.contributor.authorWestbury, Sarah K.
dc.contributor.authorWalker, Mary
dc.contributor.authorStirrups, Kathleen E
dc.contributor.authorTurro, Ernest
dc.contributor.authorChapman, Oliver
dc.contributor.authorReilly-Stitt, Christopher
dc.contributor.authorMutch, Nicola J.
dc.contributor.authorMumford, Andrew D.
dc.date.accessioned2017-07-19T23:01:14Z
dc.date.available2017-07-19T23:01:14Z
dc.date.issued2016-10-06
dc.identifier.citationBurley , 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-2016-05-716092en
dc.identifier.issn0006-4971
dc.identifier.otherPURE: 69510430
dc.identifier.otherPURE UUID: 08b01569-12f4-4162-b731-e7018b74d516
dc.identifier.otherScopus: 85030419067
dc.identifier.urihttp://hdl.handle.net/2164/8972
dc.identifier.urihttp://europepmc.org/abstract/MED/27436851en
dc.descriptionThe 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:PMC5054699en
dc.format.extent5
dc.language.isoeng
dc.relation.ispartofBlooden
dc.rightsThis research was originally published in Blood. Burley, K, Whyte, CS, Westbury, SK, Walker, M, Stirrups, KE, Turro, E, Chapman, O, Reilly-Stitt, C, Mutch, NJ & Mumford, AD., Altered fibrinolysis in autosomal dominant thrombomodulin-associated coagulopathy' Blood, Vol: 128 pp-pp. 1879-1883 © the American Society of Hematology.en
dc.subjectR Medicineen
dc.subjectMedical Research Council (MRC)en
dc.subjectMR/K023489/1en
dc.subjectBritish Heart Foundationen
dc.subjectFS/11/2/28579en
dc.subjectNational Institute for Health Research (NIHR)en
dc.subject.lccRen
dc.titleAltered fibrinolysis in autosomal dominant thrombomodulin-associated coagulopathyen
dc.typeJournal articleen
dc.contributor.institutionUniversity of Aberdeen.Institute of Medical Sciencesen
dc.contributor.institutionUniversity of Aberdeen.Applied Medicineen
dc.contributor.institutionUniversity of Aberdeen.Medical Sciences - Cardiovascular Groupen
dc.contributor.institutionUniversity of Aberdeen.Clinical Medicineen
dc.description.statusPeer revieweden
dc.description.versionPostprinten
dc.identifier.doihttps://doi.org/10.1182/blood-2016-05-716092
dc.identifier.urlhttp://europepmc.org/abstract/MED/27436851en


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