Abstract
Obsessive-compulsive disorder(OCD) is a highly disabling mental illness characterized primarily by
unnecessary compulsive thinking and behavior. In terms of genetics, abnormalities in the functions of the
serotonin, glutamate, and dopaminergic systems in the central nervous system, as well as abnormalities in
biological processes such as inflammation and intracellular signal transduction, may be related to the occurrence
and development of obsessive-compulsive disorder. Single nucleotide polymorphism may be an important reason
for these abnormalities at the molecular biology level. Therefore, studying the polymorphisms of popular
candidate genes in different pathogenesis mechanisms is crucial for analyzing the pathogenesis of
obsessive-compulsive disorder, and there is potential in predicting risk factors and accurate treatment of
obsessive-compulsive disorder.
Key words
Obsessive-compulsive disorder /
genetics /
genetic polymorphism /
single nucleotide polymorphism
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The Association between Single Nucleotide Polymorphism and Obsessive-compulsive Disorder[J]. Neural Injury and Functional Reconstruction. 0
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