Publication | Open Access

Use of next‐generation sequencing and candidate gene analysis to identify underlying defects in patients with inherited platelet function disorders

Platelet BiologyThrombosisEpidemiologyNext‐generation SequencingUnderlying DefectsBlood PlateletMedicineGeneticsHematologyPlatelet PathobiologyDisease Gene IdentificationGenomicsPublic HealthMolecular DiagnosticsCandidate Gene AnalysisCardiovascular Genetics