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Enhanced activity of human serotonin transporter variants associated with autism
Rare, functional, non-synonymous variants in the human serotonin (5-hydroxytryptamine, 5-HT) transporter (hSERT) gene (SLC6A4) have been identified in both autism and obsessive–compulsive disorder (OCD). Within autism, rare hSERT coding variants associate with rigid–compulsive traits, suggesting bot...
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| Hauptverfasser: | , , , |
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| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
The Royal Society
2008
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2674096/ https://ncbi.nlm.nih.gov/pubmed/18957375 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1098/rstb.2008.0143 |
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