Identification of a homozygous recessive variant in PTGS1 resulting in a congenital aspirin-like defect in platelet function. (2021)

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.3324/haematol.2019.235895

PubMed Identifier: 32299908

Publication URI: http://europepmc.org/abstract/MED/32299908

Type: Journal Article/Review

Volume: 106

Parent Publication: Haematologica

Issue: 5

ISSN: 0390-6078