Biochemical phenotyping of paroxysmal nocturnal hemoglobinuria reveals solute carriers and β-oxidation deficiencies

INTRODUCTION: Paroxysmal nocturnal hemoglobinuria (PNH) is a clonal disease of hematopoietic cells with a variable clinical spectrum characterized by intravascular hemolysis, high risk of thrombosis, and cytopenias. To understand the biochemical shifts underlying PNH, this study aimed to search for...

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Detalles Bibliográficos
Autores principales: Yamakawa, Patricia Eiko, Fonseca, Ana Rita, Guerreiro da Silva, Ismael Dale Cotrim, Gonçalves, Matheus Vescovi, Marchioni, Dirce Maria, Carioca, Antonio Augusto Ferreira, Michonneau, David, Arrais-Rodrigues, Celso
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2023
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10393180/
https://www.ncbi.nlm.nih.gov/pubmed/37527257
http://dx.doi.org/10.1371/journal.pone.0289285

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10393180/
https://www.ncbi.nlm.nih.gov/pubmed/37527257
http://dx.doi.org/10.1371/journal.pone.0289285

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