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

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...

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Publicat a:Dis Model Mech
Autors principals: Jumbo-Lucioni, Patricia, Parkinson, William, Broadie, Kendal
Format: Artigo
Idioma:Inglês
Publicat: The Company of Biologists Limited 2014
Matèries:
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC4257005/
https://ncbi.nlm.nih.gov/pubmed/25326312
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1242/dmm.017137
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