Overelaborated synaptic architecture and reduced synaptomatrix glycosylation in a Drosophila classic galactosemia disease model

• Hoofdauteurs: Patricia Jumbo-Lucioni (Auteur), William Parkinson (Auteur), Kendal Broadie (Auteur)
• Formaat: Boek
• Gepubliceerd in: The Company of Biologists, 2014-12-01T00:00:00Z.
• Onderwerpen: article
• Online toegang: Connect to this object online.

Classic galactosemia (CG) is an autosomal recessive disorder resulting from loss of galactose-1-phosphate uridyltransferase (GALT), which catalyzes conversion of galactose-1-phosphate and uridine diphosphate (UDP)-glucose to glucose-1-phosphate and UDP-galactose, immediately upstream of UDP-N-acetyl...