Suggestive evidence on the genetic link between mitochondria dysfunction and autism

Acta Psychiatrica Scandinavica

Volumn 123, Issue 2, 2011, Pages 95-

  Villafuerte, Sandra ^a  

^a UNIVERSITY OF MICHIGAN   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AUTISM; DISORDERS OF MITOCHONDRIAL FUNCTIONS; GENETIC LINKAGE; GENETIC VARIABILITY; HAPLOTYPE; HUMAN; NOTE; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM;

AUTISTIC DISORDER; HUMANS; MITOCHONDRIA; NADH DEHYDROGENASE; POLYMORPHISM, SINGLE NUCLEOTIDE;

EID: 78650792869     PISSN: 0001690X     EISSN: 16000447     Source Type: Journal    
DOI: 10.1111/j.1600-0447.2010.01654.x     Document Type: Note

References (2)

1. Marui T, Funatogawa I, Koishi S et al. The NADH-ubiquinone oxidoreductase 1 alpha subcomplex 5 (NDUFA5) gene variants are associated with autism. Acta Psychiatr Scand 2011;123:118-124.
2. Hass R. Autism and mitochondrial disease. Dev Disabil Res Rev 2010;16:144-153.