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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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Bibliografiske detaljer
Udgivet i:J Biol Methods
Main Authors: Brophy, Megan L., Murphy, John E., Bell, Robert D.
Format: Artigo
Sprog:Inglês
Udgivet: Journal of Biological Methods 2021
Fag:
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC8270791/
https://ncbi.nlm.nih.gov/pubmed/34258307
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.14440/jbm.2021.355
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