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Lack of association of rare functional variants in TSC1/TSC2 genes with autism spectrum disorder
BACKGROUND: Autism spectrum disorder (ASD) is reported in 30 to 60% of patients with tuberous sclerosis complex (TSC) but shared genetic mechanisms that exist between TSC-associated ASD and idiopathic ASD have yet to be determined. Through the small G-protein Rheb, the TSC proteins, hamartin and tub...
में बचाया:
| मुख्य लेखकों: | , , , , , , , |
|---|---|
| स्वरूप: | Artigo |
| भाषा: | Inglês |
| प्रकाशित: |
BioMed Central
2013
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| विषय: | |
| ऑनलाइन पहुंच: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3610211/ https://ncbi.nlm.nih.gov/pubmed/23514105 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/2040-2392-4-5 |
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