“…A plethora of studies now support this theory (for a review see: Rossignol and Frye [2012]). The overlap between autism and inherited or acquired mitochondrial disease resulting from mtDNA or nDNA mutations is less than 5% [Haas, 2010]; nevertheless, they share commonality in numerous metabolic abnormalities [Ververi et al, 2012;Ghaziuddin and Al-Owain, 2013;Gu et al, 2013;Naviaux et al, 2014;Guevara-Campos et al, 2015;Kabouridis and Pachnis, 2015], including inflammatory gastrointestinal issues [Scudellari, 2011;Wang et al, 2011;Rossignol and Frye, 2012;Chaidez et al, 2014], and both epilepsy and seizures [Wallace and Fan, 2010;Fassio et al, 2011;Scudellari, 2011;Rossignol and Frye, 2012;Novarino et al, 2012;Zafeiriou et al, 2013;Kabouridis and Pachnis, 2015;Vissoker et al, 2015].…”