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Aspartoacylase supports oxidative energy metabolism during myelination

The inherited leukodystrophy Canavan disease arises due to a loss of the ability to catabolize N-acetylaspartic acid (NAA) in the brain and constitutes a major point of focus for efforts to define NAA function. Accumulation of noncatabolized NAA is diagnostic for Canavan disease, but contrasts with...

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Detalhes bibliográficos
Main Authors: Francis, Jeremy S, Strande, Louise, Markov, Vladamir, Leone, Paola
Formato: Artigo
Idioma:Inglês
Publicado em: Nature Publishing Group 2012
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3434629/
https://ncbi.nlm.nih.gov/pubmed/22617649
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/jcbfm.2012.66
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