טוען...
The genetic and neurobiologic compass points toward common signaling dysfunctions in autism spectrum disorders
Autism spectrum disorder (ASD) is a common neurodevelopmental disorder with high heritability. Here, we discuss data supporting the view that there are at least two distinct genetic etiologies for ASD: rare, private (de novo) single gene mutations that may have a large effect in causing ASD; and inh...
שמור ב:
| Main Authors: | , |
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| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
American Society for Clinical Investigation
2009
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2662567/ https://ncbi.nlm.nih.gov/pubmed/19339766 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1172/JCI37934 |
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