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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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| Veröffentlicht in: | J Biol Methods |
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| Hauptverfasser: | , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
Journal of Biological Methods
2021
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| Schlagworte: | |
| Online Zugang: | 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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