Chan MV, Hayman MA, Suthesh Sivapalaratnam, Marilena Crescente, Allan HE, Edin ML, Zeldin DC, Milne GL, Jonathan Stephens, Daniel Greene, Moghees Hanif, O’Donnell VB, Liang Dong, Malkowski MG, Claire Lentaigne, Katherine Wedderburn, Matthew Stubbs, Kate Downes, Ouwehand WH, Ernest Turro, NIHR BioResource, Hart DP, Kathleen Freson, Laffan MA, Warner TD. Identification of a homozygous recessive variant in <i>PTGS1</i&gt; resulting in a congenital aspirin-like defect in platelet function. haematol [Internet]. 2021Apr.30 [cited 2024Apr.24];106(5):1423-32. Available from: https://haematologica.org/article/view/9716