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A large-scale screen for coding variants in SERT/SLC6A4 in autism spectrum disorders
In the current study we explored the hypothesis that rare variants in SLC6A4 contribute to autism susceptibility and to rigid-compulsive behaviors in autism. We made use of a large number of unrelated cases with autism spectrum disorders (∼350) and controls (∼420) and screened for rare exonic varian...
Sparad:
| Huvudupphovsmän: | , , , , , , |
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| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
2008
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| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2678895/ https://ncbi.nlm.nih.gov/pubmed/19360675 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/aur.30 |
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