Title : Glutaric aciduria type 1 metabolites impair the succinate transport from astrocytic to neuronal cells.

Pub. Date : 2011 May 20

PMID : 21454630






2 Functional Relationships(s)
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Protein Name
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1 The inherited neurodegenerative disorder glutaric aciduria type 1 (GA1) results from mutations in the gene for the mitochondrial matrix enzyme glutaryl-CoA dehydrogenase (GCDH), which leads to elevations of the dicarboxylates glutaric acid (GA) and 3-hydroxyglutaric acid (3OHGA) in brain and blood. 3-hydroxyglutaric acid glutaryl-Coenzyme A dehydrogenase Mus musculus
2 The inherited neurodegenerative disorder glutaric aciduria type 1 (GA1) results from mutations in the gene for the mitochondrial matrix enzyme glutaryl-CoA dehydrogenase (GCDH), which leads to elevations of the dicarboxylates glutaric acid (GA) and 3-hydroxyglutaric acid (3OHGA) in brain and blood. 3-hydroxyglutaric acid glutaryl-Coenzyme A dehydrogenase Mus musculus