Cargando…
IRIDA Phenotype in TMPRSS6 Monoallelic-Affected Patients: Toward a Better Understanding of the Pathophysiology
Iron-refractory iron deficiency anemia (IRIDA) is an autosomal recessive inherited form of iron deficiency anemia characterized by discrepantly high hepcidin levels relative to body iron status. However, patients with monoallelic exonic TMPRSS6 variants have also been reported to express the IRIDA p...
Autores principales: | Hoving, Vera, Korman, Scott E., Antonopoulos, Petros, Donker, Albertine E., Schols, Saskia E. M., Swinkels, Dorine W. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9331965/ https://www.ncbi.nlm.nih.gov/pubmed/35893046 http://dx.doi.org/10.3390/genes13081309 |
Ejemplares similares
-
A novel TMPRSS6 mutation that prevents protease auto-activation causes IRIDA
por: Altamura, Sandro, et al.
Publicado: (2010) -
One-pot syntheses of irida-polycyclic aromatic hydrocarbons
por: Hu, Yu Xuan, et al.
Publicado: (2019) -
Correction: One-pot syntheses of irida-polycyclic aromatic hydrocarbons
por: Hu, Yu Xuan, et al.
Publicado: (2019) -
Transferrin Saturation/Hepcidin Ratio Discriminates TMPRSS6-Related Iron Refractory Iron Deficiency Anemia from Patients with Multi-Causal Iron Deficiency Anemia
por: van der Staaij, Hilde, et al.
Publicado: (2022) -
Formation
of Irida-β-ketoimines and PCN(amine)-Ir(III) Complexes
by Reacting Irida-β-diketones
with Aliphatic Diamines: Catalytic Activity in Hydrogen Release by
Methanolysis of H(3)N–BH(3)
por: Bustos, Itxaso, et al.
Publicado: (2022)