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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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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

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