Biochemical phenotyping of paroxysmal nocturnal hemoglobinuria reveals solute carriers and [beta]-ox...
Biochemical phenotyping of paroxysmal nocturnal hemoglobinuria reveals solute carriers and [beta]-oxidation deficiencies
About this item
Full title
Author / Creator
Publisher
Public Library of Science
Journal title
Language
English
Formats
Publication information
Publisher
Public Library of Science
Subjects
More information
Scope and Contents
Contents
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 the dysfunctional pathways involved in PNH physiopathology by co...
Alternative Titles
Full title
Biochemical phenotyping of paroxysmal nocturnal hemoglobinuria reveals solute carriers and [beta]-oxidation deficiencies
Authors, Artists and Contributors
Identifiers
Primary Identifiers
Record Identifier
TN_cdi_gale_infotracmisc_A759254671
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_gale_infotracmisc_A759254671
Other Identifiers
ISSN
1932-6203
E-ISSN
1932-6203
DOI
10.1371/journal.pone.0289285