Red Blood Cell Metabolism in Pyruvate Kinase Deficient Patients

Background: Pyruvate kinase deficiency (PKD) is the most frequent congenital enzymatic defect of glycolysis, and one of the most common causes of hereditary non spherocytic hemolytic anemia. Therapeutic interventions are limited, in part because of the incomplete understanding of the molecular mecha...

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Detalles Bibliográficos
Autores principales: Roy, Micaela K., Cendali, Francesca, Ooyama, Gabrielle, Gamboni, Fabia, Morton, Holmes, D’Alessandro, Angelo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Physiology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8567077/
https://www.ncbi.nlm.nih.gov/pubmed/34744776
http://dx.doi.org/10.3389/fphys.2021.735543

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8567077/
https://www.ncbi.nlm.nih.gov/pubmed/34744776
http://dx.doi.org/10.3389/fphys.2021.735543

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