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Updated: Feb 13, 2026

Eye Tracking Young Children with Autism
Published on: March 27, 2012
Association Study Between Metallothionein-3 Protein Polymorphisms and Autism
MingXia Yu1, Tao Cao2, Dan Yu1
1Center for Gene Diagnosis, Zhongnan Hospital of Wuhan University, No. 169, East Lake Road, Wuchang District, Wuhan, 430071, Hubei, People's Republic of China.
Genetic variations in the Metallothionein III (MT3) gene were investigated as a potential risk factor for autism. This study found no association between MT3 gene polymorphisms and autism risk in children.
Area of Science:
- Neurogenetics
- Environmental Health
Background:
- High mercury body burden is a suspected autism risk factor.
- Metallothionein III (MT3) is a brain-specific protein crucial for metal metabolism.
Purpose of the Study:
- To investigate potential genetic variations in the MT3 gene associated with autism predisposition.
- To determine if MT3 gene polymorphisms correlate with autism risk.
Main Methods:
- Analyzed nine single nucleotide polymorphisms (SNPs) in the MT3 gene from 132 autistic children and 132 controls.
- Assessed MT3 mRNA levels in white blood cells using real-time PCR.
- Identified four novel MT3 SNPs not previously recorded in the human SNP database.
Main Results:
- No association was found between the studied MT3 polymorphisms and MT3 mRNA levels.
- No significant association was detected between MT3 gene polymorphisms and the risk of autism.
- Four previously undocumented MT3 SNPs were discovered.
Conclusions:
- MT3 gene polymorphisms do not appear to be associated with autism risk.
- Further research is needed to determine the clinical significance of the novel MT3 SNPs identified.
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