Publication:
Corrigendum to Diagnosis and management of severe congenital protein C deficiency (SCPCD): Communication from the SSC of the ISTH [J Thromb Haemost. 2022 Jul;20(7):1735-1743] (Journal of Thrombosis and Haemostasis (2022) 20(7) (1735–1743), (S1538783622019237), (10.1111/jth.15732))

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dc.contributor.authorMinford, Adrian (6602893631)
dc.contributor.authorBrandão, Leonardo R. (12788818600)
dc.contributor.authorOthman, Maha (7006122614)
dc.contributor.authorMale, Christoph (7003604062)
dc.contributor.authorAbdul-Kadir, Rezan (7004016849)
dc.contributor.authorMonagle, Paul (7004308240)
dc.contributor.authorMumford, Andrew D. (57202968151)
dc.contributor.authorAdcock, Dorothy (7003902745)
dc.contributor.authorDahlbäck, Björn (7103328699)
dc.contributor.authorMiljic, Predrag (6604038486)
dc.contributor.authorDeSancho, Maria T. (11138767900)
dc.contributor.authorTeruya, Jun (8679464900)
dc.date.accessioned2025-06-12T12:18:17Z
dc.date.available2025-06-12T12:18:17Z
dc.date.issued2023
dc.description.abstractThe authors regret the affiliation of Clinical Pathology Department, Faculty of Medicine, Mansoura University, Egypt was omitted for Maha Othman. This has been corrected and added as below. The authors would like to apologise for any inconvenience caused. © 2023
dc.identifier.urihttps://doi.org/10.1016/j.jtha.2023.01.019
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85150260035&doi=10.1016%2fj.jtha.2023.01.019&partnerID=40&md5=678f99201e7abf81bc1544578691ddf2
dc.identifier.urihttps://remedy.med.bg.ac.rs/handle/123456789/2805
dc.titleCorrigendum to Diagnosis and management of severe congenital protein C deficiency (SCPCD): Communication from the SSC of the ISTH [J Thromb Haemost. 2022 Jul;20(7):1735-1743] (Journal of Thrombosis and Haemostasis (2022) 20(7) (1735–1743), (S1538783622019237), (10.1111/jth.15732))
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