Publication | Open Access

Next‐generation sequencing study finds an excess of rare, coding single‐nucleotide variants of ADAMTS13 in patients with deep vein thrombosis

ThrombosisVenous ThrombosisSequencingMedicineGeneticsDeep Vein ThrombosisHematologyGenetic EpidemiologyPathologySingle‐nucleotide VariantsGenomicsMolecular DiagnosticsBioinformaticsVariant Interpretation