ヒドロキシグルタル酸尿症
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English Journal
- Glutaric aciduria type 1 metabolites impair the succinate transport from astrocytic to neuronal cells.
- Lamp J, Keyser B, Koeller DM, Ullrich K, Braulke T, Muhlhausen C.SourceFrom the Children's Hospital, Department of Biochemistry, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany and.
- The Journal of biological chemistry.2011 May 20;286(20):17777-84. Epub 2011 Mar 29.
- 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.
- PMID 21454630
Japanese Journal
- Founder effect confirmation of c.241A>G mutation in the L2HGDH gene and characterization of oxidative stress parameters in six Tunisian families with L-2-hydroxyglutaric aciduria
- L-2-Hydroxyglutaric aciduria presenting with severe autistic features
- 遺伝子解析により確定診断した L-2-hydroxyglutaric aciduria の1例
Related Links
- 2-hydroxyglutaric aciduria is a condition that causes progressive damage to the brain. The major types of this disorder are called D-2-hydroxyglutaric aciduria (D-2-HGA), L-2-hydroxyglutaric aciduria (L-2-HGA), and ...
- 2-hydroxyglutaric aciduria is a condition that causes progressive damage to the brain. The major types of this disorder are called D-2-hydroxyglutaric aciduria (D-2-HGA), L-2-hydroxyglutaric aciduria (L-2-HGA), and combined D,L-2 ...
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- 英
- hydroxyglutaric aciduria