Identification of a homozygous recessive variant in PTGS1 resulting in a congenital aspirin-like defect in platelet function.

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Bibliographic Details
Title: Identification of a homozygous recessive variant in PTGS1 resulting in a congenital aspirin-like defect in platelet function.
Authors: Chan MV; Queen Mary, University of London., Hayman MA; Queen Mary, University of London., Sivapalaratnam S; University of Cambridge., Crescente M; Queen Mary, University of London., Allan HE; Queen Mary, University of London., Edin ML; National Institutes of Health, National Institute of Environmental Health Sciences., Zeldin DC; National Institutes of Health, National Institute of Environmental Health Sciences., Milne GL; Vanderbilt University Medical Center., Stephens J; University of Cambridge., Greene D; University of Cambridge., Hanif M; Barts Health National Health Service Trust., O'Donnell VB; Cardiff University., Dong L; University of Buffalo., Malkowski MG; University of Buffalo., Lentaigne C; Imperial College Healthcare National Health Service Trust., Wedderburn K; University of Cambridge., Stubbs M; Imperial College Healthcare National Health Service Trust., Downes K; University of Cambridge., Ouwehand WH; University of Cambridge National Blood Service Centre., Turro E; University of Cambridge., BioResource N, Hart DP; Queen Mary University of London., Freson K; University of Leuven., Laffan MA; Imperial College London., Warner TD; Queen Mary University of London.
Source: Haematologica [Haematologica] 2021 May 01; Vol. 106 (5), pp. 1423-1432. Date of Electronic Publication: 2021 May 01.
Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, N.I.H., Intramural; Research Support, Non-U.S. Gov't
Journal Info: Publisher: Ferrata Storti Foundation Country of Publication: Italy NLM ID: 0417435 Publication Model: Electronic Cited Medium: Internet ISSN: 1592-8721 (Electronic) Linking ISSN: 03906078 NLM ISO Abbreviation: Haematologica Subsets: MEDLINE
Database: MEDLINE Ultimate
Description
ISSN:1592-8721
DOI:10.3324/haematol.2019.235895