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Updated: Jan 26, 2026

In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila
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In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila

Published on: August 20, 2019

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A functional variant in SLC1A3 influences ADHD risk by disrupting a hsa-miR-3171 binding site: A two-stage

Xin Huang1,2, Qi Zhang1,2, Xinzhen Chen1,2

  • 1Key Laboratory of Environment and Health, Ministry of Education & Ministry of Environmental Protection, School of Public Health, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, People's Republic of China.

Genes, Brain, and Behavior
|April 7, 2019
PubMed

Keywords:
SLC1A3 geneADHDassociation studydual-luciferase reporter assay

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