Completed Heart, Stroke & Blood Genetics & Molecular Biology
Mapping and functional investigation of genetic mutations in patients with mild, platelet bleeding disorders
About this grant
This summary is based on the grant title only — the full abstract was not available.
Research project funded by BHF at University of Birmingham.
View the original record at the funder ↗
Researchers
Stephen Watson (EPMC Awardee)
Related Research
Grants with similar aims, by meaning.
Identification and functional investigation of genes in patients with inherited bleeding disorders (Miss Annabel MacLachlan)
Mild bleeding disorders caused by platelet defects
Molecular and Structural characterisation of rare GPCR genetic variants in patients with impaired haemostasis
Genotyping and Phenotyping of Platelets. (GAPP)
Genetic analysis of platelets in healthy individuals
Original classification
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