Altered fibrinolysis in autosomal dominant thrombomodulin associated coagulopathy
| Contribuinte(s) |
University of Aberdeen, Medicine, Medical Sciences & Nutrition, Applied Medicine University of Aberdeen, Medical Sciences - Cardiovascular Group |
|---|---|
| Data(s) |
05/08/2016
05/08/2016
19/07/2016
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| Resumo |
The 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. Peer reviewed Postprint |
| Identificador |
Burley , 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 . , 10.1182/blood-2016-05-716092 0006-4971 PURE: 69510430 PURE UUID: 08b01569-12f4-4162-b731-e7018b74d516 |
| Idioma(s) |
eng |
| Relação |
Blood |
| Direitos |
© Blood Online by the American Society of Hematology |
| Palavras-Chave | #R Medicine #Medical Research Council (MRC) #MR/K023489/1 #British Heart Foundation #FS/11/2/28579 #R |
| Tipo |
Journal article |
