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Unique acyl-carnitine profiles are potential biomarkers for acquired mitochondrial disease in autism spectrum disorder

Autism spectrum disorder (ASD) has been associated with mitochondrial disease (MD). Interestingly, most individuals with ASD and MD do not have a specific genetic mutation to explain the MD, raising the possibility of that MD may be acquired, at least in a subgroup of children with ASD. Acquired MD...

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Detalhes bibliográficos
Main Authors: Frye, R E, Melnyk, S, MacFabe, D F
Formato: Artigo
Idioma:Inglês
Publicado em: Nature Publishing Group 2013
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3566723/
https://ncbi.nlm.nih.gov/pubmed/23340503
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/tp.2012.143
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