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Updated: Aug 24, 2026

A Method to Study the C924T Polymorphism of the Thromboxane A2 Receptor Gene
Published on: April 1, 2019
Hunting for the mutation in inherited thrombophilia
Keith Gomez1, Michael A Laffan
1MRC Clinical Sciences Centre, Imperial College School of Medicine, Hammersmith Hospital, London, UK. keith.gomez@csc.mrc.ac.uk
Abstract:
Mutation detection in inherited thrombophilia remains largely confined to the research laboratory. However, there are specific situations when investigating the genetic defect causing thrombophilia can provide additional useful clinical information. This review discusses the value of genetic analysis in the common inherited thrombophilias.
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