Identification of a homozygous recessive variant in PTGS1 resulting in a congenital aspirin-like defect in platelet function. - Chan MV; Hayman MA; Sivapalaratnam S; Crescente M; Allan HE; Edin ML; Zeldin DC; Milne GL; Stephens J; Greene D; Hanif M; O'Donnell VB; et al. (Haematologica, 2021)