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The aim of this study was to describe the association between autism and the mitochondrial aspartate/glutamate carrier SLC25A12 gene on chromosome 2q31
Abstract:
OBJECTIVE: Autism is a neurodevelopmental disorder with childhood onset and a known major genetic component. A recent study identified a highly significant association between autism and a two-single-nucleotide-polymorphism haplotype in the SLC25A12 gene, with a homozygote genotype relative risk between 2.4 and 4.8. The authors' goal was to investigate this association with autism in more...
International Classification:
Mental and behavioural disorders - Disorders of psychological development - autism
Categories:
autism
Geography:
Republic of Ireland
Am J Psychiatry,
Vol: 162 Page: 2182-4 November 2005
R. Segurado; J. Conroy; E. Meally; M. Fitzgerald; M. Gill; L. Gallagher
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