Barely Significant
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Candidate Genes and Pathways Associated with Gilles de la Tourette Syndrome-Where Are We?

Genes (Basel) · 2021 · PMC8468358 · PMID 34573303

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nominally significantno p-value reported
In 2010, common polymorphisms in several serotonin receptors ( HTR1A , HTR2A , and HTR2C ) were investigated in 87 Caucasian GTS individuals and 311 controls, and only the HTR2C polymorphisms Cys759Thr and Gly697Cys showed a nominally significant association with GTS [ 51 ].

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