Comprehensive functional characterisation of a novel ANO6 variant in a new patient with Scott Syndrome

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• Finished

  Investigating the role of SLFN14 in megakaryocyte and platelet biology

  Morgan, N. & Watson, S.

  British Heart Foundation

  4/06/18 → 3/06/21

  Project: Research

  • Blood Platelets 100%
  • Hemorrhage 72%
  • Scott Syndrome 61%
  • Genes 45%
  • Tropomyosin 41%

• Functional investigation of SLFN14 in megakaryocyte and platelet biology

  Morgan, N. & Gough, R.

  British Heart Foundation

  22/08/17 → 20/02/20

  Project: Research

  • Blood Platelets 100%
  • Hemorrhage 72%
  • Scott Syndrome 61%
  • Genes 45%
  • Tropomyosin 41%

• Identification and functional investigation of genes in patients with inherited bleeding disorders

  Morgan, N. & Watson, S.

  British Heart Foundation

  28/09/15 → 27/09/18

  Project: Research

  • Blood Platelets 100%
  • Hemorrhage 50%
  • Scott Syndrome 35%
  • Genes 25%
  • Whole Exome Sequencing 24%

• Molecular Genetic Investigation of Patients with Congenital Thrombocytopenias

  Morgan, N., Harrison, P., Lowe, G. & Watson, S.

  British Heart Foundation

  18/11/13 → 17/11/16

  Project: Research

  • Blood Platelets 100%
  • Thrombocytopenia 58%
  • Hemorrhage 46%
  • Whole Exome Sequencing 37%
  • Genes 26%