Primary Hyperoxaluria

Primary hyperoxalurias (PH) are inborn errors in the metabolism of glyoxylate and oxalate. PH type 1, the most common form, is an autosomal recessive disorder caused by a deficiency of the liver-specific enzyme alanine, glyoxylate aminotransferase (AGT) resulting in overproduction and excessive urin...

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Detalles Bibliográficos
Autores principales: Harambat, Jérôme, Fargue, Sonia, Bacchetta, Justine, Acquaviva, Cécile, Cochat, Pierre
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE-Hindawi Access to Research 2011
Materias:
Review Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3124893/
https://www.ncbi.nlm.nih.gov/pubmed/21748001
http://dx.doi.org/10.4061/2011/864580

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3124893/
https://www.ncbi.nlm.nih.gov/pubmed/21748001
http://dx.doi.org/10.4061/2011/864580

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