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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...
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 |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2023
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Materias: | |
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 |
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