Assessment of galactose-1-phosphate uridyltransferase activity in cells and tissues

Galactosemias are a family of autosomal recessive genetic disorders resulting from impaired enzymes of the Leloir pathway of galactose metabolism including galactokinase, galactose uridyltransferase, and UDP-galactose 4-epimerase that are critical for conversion of galactose into glucose-6-phosphate...

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Detalles Bibliográficos
Autores principales: Brophy, Megan L., Murphy, John E., Bell, Robert D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Journal of Biological Methods 2021
Materias:
Protocol
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8270791/
https://www.ncbi.nlm.nih.gov/pubmed/34258307
http://dx.doi.org/10.14440/jbm.2021.355

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8270791/
https://www.ncbi.nlm.nih.gov/pubmed/34258307
http://dx.doi.org/10.14440/jbm.2021.355

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