Palma-Barqueros, Verónica, Crescente, Marilena ORCID: https://orcid.org/0000-0003-3164-512X, de la Morena, María Eugenia, Chan, Melissa V, Almarza, Elena, Revilla, Nuria, Bohdan, Natalia, Miñano, Antonia, Padilla, José, Allan, Harriet E, Maffucci, Tania, Edin, Matthew L, Zeldin, Darryl C, Mesa-Nuñez, Cristina, Damian, Carlos, Marín-Quilez, Ana, Benito, Rocío, Martínez-Martínez, Irene, Bermejo, Nuria, Casas-Aviles, Ignacio, Rodríguez-Alen, Agustín, González-Porras, José R, Hernández-Rivas, Jesús María, Vicente, Vicente, Corral, Javier, Lozano, María L, Warner, Timothy D, Bastida, José María and Rivera, José
(2020)
A novel genetic variant in PTGS1 affects N-glycosylation of cyclooxygenase-1 causing a dominant-negative effect on platelet function and bleeding diathesis.
American Journal of Hematology, 96 (3).
E83-E88.
ISSN 0361-8609
Item Type: |
Article
|
Peer-reviewed: |
Yes
|
Date Deposited: |
01 Jul 2021 10:49
|
Publisher: |
Wiley |
Divisions: |
Faculties > Science and Engineering Research Centres > Centre for Bioscience |
Subject terms: |
Humans, Hemorrhagic Disorders, Protein Processing, Post-Translational, Glycosylation, Platelet Activation, Heterozygote, Genes, Dominant, Phenotype, Mutation, Missense, Adolescent, Asian Continental Ancestry Group, Female, Cyclooxygenase 1, HEK293 Cells, Loss of Function Mutation, Humans, Hemorrhagic Disorders, Protein Processing, Post-Translational, Glycosylation, Platelet Activation, Heterozygote, Genes, Dominant, Phenotype, Mutation, Missense, Adolescent, Asian Continental Ancestry Group, Female, Cyclooxygenase 1, HEK293 Cells, Loss of Function Mutation, Adolescent, Asian Continental Ancestry Group, Cyclooxygenase 1, Female, Genes, Dominant, Glycosylation, HEK293 Cells, Hemorrhagic Disorders, Heterozygote, Humans, Loss of Function Mutation, Mutation, Missense, Phenotype, Platelet Activation, Protein Processing, Post-Translational, 1102 Cardiorespiratory Medicine and Haematology, Immunology |
URI: |
https://mmu-uat.leaf.cosector.com/id/eprint/628010 |
DOI: |
https://doi.org/10.1002/ajh.26076 |
ISSN |
0361-8609 |
e-ISSN |
1096-8652 |
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