Pathophysiology and targets for treatment in hereditary galactosemia: A systematic review of animal and cellular models

Since the first description of galactosemia in 1908 and despite decades of research, the pathophysiology is complex and not yet fully elucidated. Galactosemia is an inborn error of carbohydrate metabolism caused by deficient activity of any of the galactose metabolising enzymes. The current standard...

Descripción completa

Detalles Bibliográficos
Autores principales: Haskovic, Minela, Coelho, Ana I., Bierau, Jörgen, Vanoevelen, Jo M., Steinbusch, Laura K. M., Zimmermann, Luc J. I., Villamor‐Martinez, Eduardo, Berry, Gerard T., Rubio‐Gozalbo, M. Estela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2020
Materias:
Review Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7317974/
https://www.ncbi.nlm.nih.gov/pubmed/31808946
http://dx.doi.org/10.1002/jimd.12202

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7317974/
https://www.ncbi.nlm.nih.gov/pubmed/31808946
http://dx.doi.org/10.1002/jimd.12202

Ejemplares similares