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Identification of a homozygous recessive variant in PTGS1 r..:
Chan, Melissa V.
;
Hayman, Melissa A.
;
Suthesh Sivapalaratnam
...
Haematologica. 106 (2020) 5 - p. 1423-1432 , 2020
Link:
https://doi.org/10.3324/haematol.2019.235895
RT Journal T1
Identification of a homozygous recessive variant in PTGS1 resulting in a congenital aspirin-like defect in platelet function
UL https://suche.suub.uni-bremen.de/peid=cr-10.3324_haematol.2019.235895&Exemplar=1&LAN=DE A1 Chan, Melissa V. A1 Hayman, Melissa A. A1 Suthesh Sivapalaratnam A1 Marilena Crescente A1 Allan, Harriet E. A1 Edin, Matthew L. A1 Zeldin, Darryl C. A1 Milne, Ginger L. A1 Jonathan Stephens A1 Daniel Greene A1 Moghees Hanif A1 O'Donnell, Valerie B. A1 Liang Dong A1 Malkowski, Michael G. A1 Claire Lentaigne A1 Katherine Wedderburn A1 Matthew Stubbs A1 Kate Downes A1 Ouwehand, Willem H. A1 Ernest Turro A1 NIHR BioResource A1 Hart, Daniel P. A1 Kathleen Freson A1 Laffan, Michael A. A1 Warner, Timothy D. PB Ferrata Storti Foundation (Haematologica) YR 2020 SN 1592-8721 SN 0390-6078 JF Haematologica VO 106 IS 5 SP 1423 OP 1432 LK http://dx.doi.org/https://doi.org/10.3324/haematol.2019.235895 DO https://doi.org/10.3324/haematol.2019.235895 SF ELIB - SuUB Bremen
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