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• W2086576625 startingPage "144" @default.
• W2086576625 abstract "Autism spectrum disorder (ASD) as defined by the revised Diagnostic and Statistical Manual of Mental Disorders: DSM IVTR criteria (American Psychiatric Association [2000] Washington, DC: American Psychiatric Publishing) as impairment before the age of 3 in language development and socialization with the development of repetitive behaviors, appears to be increased in incidence and prevalence. Similarly, mitochondrial disorders are increasingly recognized. Although overlap between these disorders is to be expected, accumulating clinical, genetic, and biochemical evidence suggests that mitochondrial dysfunction in ASD is more commonly seen than expected. Some patients with ASD phenotypes clearly have genetic-based primary mitochondrial disease. This review will examine the data linking autism and mitochondria. © 2010 Wiley-Liss, Inc. Dev Disabil Res Rev 2010;16:144–153." @default.
• W2086576625 created "2016-06-24" @default.
• W2086576625 creator A5088673881 @default.
• W2086576625 date "2010-08-27" @default.
• W2086576625 modified "2023-09-26" @default.
• W2086576625 title "Autism and mitochondrial disease" @default.
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• W2086576625 doi "https://doi.org/10.1002/ddrr.112" @default.
• W2086576625 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/20818729" @default.
• W2086576625 hasPublicationYear "2010" @default.
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