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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...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: Salyer, William R., Salyer, Diane C.
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: 1974
Gaiak:
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC475395/
https://ncbi.nlm.nih.gov/pubmed/4371254
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