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Thiamine deficiency and oxalosis

Type I hyperoxaluria results from reduced activity of α-ketoglutarate: glyoxylate carboligase, which is necessary for the synergistic decarboxylation of glyoxylate and α-ketoglutarate to α-hydroxy-β-keto-adipate. Since thiamine pyrophosphate is a cofactor in the reaction, thiamine deficiency might b...

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Bibliografische gegevens
Gepubliceerd in:J Clin Pathol
Hoofdauteurs: Salyer, William R., Salyer, Diane C.
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: BMJ Publishing Group 1974
Onderwerpen:
Online toegang:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC475395/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/4371254/
https://ncbi.nlm.nih.govhttps://doi.org/10.1136/jcp.27.7.558
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