Cargando...
Inherited propionyl-CoA carboxylase deficiency in “ketotic hyperglycinemia”
Cultured fibroblasts from a young girl with ketotic hyperglycinemia were unable to oxidize propionate-(14)C to (14)CO(2), but oxidized methylmalonate-(14)C and succinate-(14)C normally. This block in propionate catabolism was shown to result from a lack of propionyl-CoA carboxylase activity. The car...
Guardado en:
| Publicado en: | J Clin Invest |
|---|---|
| Autores principales: | , , |
| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
American Society for Clinical Investigation
1971
|
| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC291900/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/5101292/ https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI106466 |
| Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|