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Platelets Volume 32, 2021 - Issue 5
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Gene of the issue

PTGS1 gene variations associated with bleeding and platelet dysfunction

Verónica Palma-Barqueros1 Universidad de Murcia, IMIB-Arrixaca, CIBERER-U765, Murcia, SpainORCID Iconhttps://orcid.org/0000-0002-5699-0053View further author information
ORCID Icon,
Natalia Bohdan1 Universidad de Murcia, IMIB-Arrixaca, CIBERER-U765, Murcia, SpainView further author information
,
Nuria Revilla1 Universidad de Murcia, IMIB-Arrixaca, CIBERER-U765, Murcia, SpainView further author information
,
Vicente Vicente1 Universidad de Murcia, IMIB-Arrixaca, CIBERER-U765, Murcia, SpainView further author information
,
José M. Bastida2 Department of Hematology, IBSAL-Hospital Universitario de Salamanca, Salamanca, Spain;3 On Behalf of the “Inherited Platelet Disorders Project”, Hemorrhagic Diathesis Working Group, SETHORCID Iconhttps://orcid.org/0000-0002-8007-3909View further author information
ORCID Icon &
José Rivera1 Universidad de Murcia, IMIB-Arrixaca, CIBERER-U765, Murcia, Spain;3 On Behalf of the “Inherited Platelet Disorders Project”, Hemorrhagic Diathesis Working Group, SETHCorrespondence[email protected]
View further author information
Pages 710-716 | Received 19 Apr 2020, Accepted 05 Jun 2020, Published online: 25 Jun 2020
 
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Author Contributions

VPM, NR, JMB & JR wrote the manuscript. NB helped in the figures and tables. All authors critically reviewed the paper.

Disclosure Of Conflict Of Interest

The authors declare no conflict of interest.

Additional information

Funding

This work was partially supported by grants from Instituto de Salud Carlos III (ISCIII) & Feder [PI17/01311, PI17/01966 and CB15/00055], Fundación Séneca [19873/GERM/15], Gerencia Regional de Salud [GRS 2061A/19 and 1647/A/17], Fundación Mutua Madrileña [FMM, AP172142019] and Sociedad Española de Trombosis y Hemostasia (SETH-FETH; Premio López Borrasca 2019 y Ayuda a Grupos de Trabajo en Patología Hemorrágica 2019). The authors research in Inherited Platelet Disorders is conducted according to the aims of the Project “Functional and Molecular Characterization of Patients with Inherited Platelet Disorders” supported by the Hemorrhagic Diathesis Working Group of the Spanish Society of Thrombosis and Haemostasis.

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