Deficiency of 2-oxo-glutarate: glyoxylate carboligase activity in primary hyperoxaluria.
AUTOR(ES)
Koch, J
ACESSO AO ARTIGO
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=224664Documentos Relacionados
- Mistargeting of peroxisomal L-alanine:glyoxylate aminotransferase to mitochondria in primary hyperoxaluria patients depends upon activation of a cryptic mitochondrial targeting sequence by a point mutation.
- Primary hyperoxaluria type 1 in the Canary Islands: A conformational disease due to I244T mutation in the P11L-containing alanine:glyoxylate aminotransferase
- Crystals in brain and meninges in primary hyperoxaluria and oxalosis.
- A clinicopathological study of ocular involvement in primary hyperoxaluria type I.
- Iron-Mediated Degradation of IRP2, an Unexpected Pathway Involving a 2-Oxoglutarate-Dependent Oxygenase Activity