Ammonium Accumulation and Cell Death in a Rat 3D Brain Cell Model of Glutaric Aciduria Type I

Glutaric aciduria type I (glutaryl-CoA dehydrogenase deficiency) is an inborn error of metabolism that usually manifests in infancy by an acute encephalopathic crisis and often results in permanent motor handicap. Biochemical hallmarks of this disease are elevated levels of glutarate and 3-hydroxygl...

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Detalles Bibliográficos
Autores principales: Jafari, Paris, Braissant, Olivier, Zavadakova, Petra, Henry, Hugues, Bonafé, Luisa, Ballhausen, Diana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3542363/
https://www.ncbi.nlm.nih.gov/pubmed/23326493
http://dx.doi.org/10.1371/journal.pone.0053735

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3542363/
https://www.ncbi.nlm.nih.gov/pubmed/23326493
http://dx.doi.org/10.1371/journal.pone.0053735

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