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OC 78.4 : Haemorrhagic sub-phenotypes in hereditary haemorrhagic telangiectasia are associated with high impact DNA variants in platelet/coagulation genes responsible for general population bleeding disorders

Researchers

Presenter

  • K. Joyce

Principal Investigators

  • F. Nur

  • G. Thomas

  • T. Ferguson

  • C. Millar

  • N. Cooper

  • M. Layton

  • M. Caulfield

Medical Centers

  • Imperial College School of Medicine, London, England, United Kingdom

  • Imperial College Healthcare NHS Foundation Trust, London, England, United Kingdom

  • NCRI and Imperial College London, London, United Kingdom

  • Genomics England, London, United Kingdom

Locations

  • United Kingdom

Companies

  • N/A

Study Components

Therapeutic Area

  • N/A

Disease

  • N/A

Biomarkers

  • N/A

Drug/Treatment

  • N/A

Outcome

  • N/A


Study Design

  • Double Blind/Blinded

Phase

  • NA

Study Id's

  • N/A

Sponsors

  • N/A

Result

  • N/A