Transferrin Isoforms, Old but New Biomarkers in Hereditary Fructose Intolerance

Hereditary Fructose Intolerance (HFI) is an autosomal recessive inborn error of metabolism characterised by the deficiency of the hepatic enzyme aldolase B. Its treatment consists in adopting a fructose-, sucrose-, and sorbitol (FSS)-restrictive diet for life. Untreated HFI patients present an abnor...

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Detalles Bibliográficos
Autores principales: Cano, Ainara, Alcalde, Carlos, Belanger-Quintana, Amaya, Cañedo-Villarroya, Elvira, Ceberio, Leticia, Chumillas-Calzada, Silvia, Correcher, Patricia, Couce, María Luz, García-Arenas, Dolores, Gómez, Igor, Hernández, Tomás, Izquierdo-García, Elsa, Martínez Chicano, Dámaris, Morales, Montserrat, Pedrón-Giner, Consuelo, Petrina Jáuregui, Estrella, Peña-Quintana, Luis, Sánchez-Pintos, Paula, Serrano-Nieto, Juliana, Unceta Suarez, María, Vitoria Miñana, Isidro, de las Heras, Javier
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8267838/
https://www.ncbi.nlm.nih.gov/pubmed/34208868
http://dx.doi.org/10.3390/jcm10132932

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8267838/
https://www.ncbi.nlm.nih.gov/pubmed/34208868
http://dx.doi.org/10.3390/jcm10132932

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