Publication | Open Access

Identification of a novel point mutation in platelet glycoprotein Ibα, Gly to Ser at residue 233, in a Japanese family with platelet-type von Willebrand disease

ThrombosisBlood PlateletGenetic DisorderJapanese FamilyGeneticsPathogenesisInherited Metabolic DiseaseHematologyPathologyHemostasisMolecular GeneticsBleeding DisorderPlatelet Glycoprotein IbαMedicineNovel Point Mutation