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Region-specific alterations in brain development in one- to three-year-old boys with fragile X syndrome
Longitudinal neuroimaging investigation of fragile X syndrome (FXS), the most common cause of inherited intellectual disability and autism, provides an opportunity to study the influence of a specific genetic factor on neurodevelopment in the living human brain. We examined voxel-wise gray and white...
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| Hlavní autoři: | , , , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
National Academy of Sciences
2010
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2889103/ https://ncbi.nlm.nih.gov/pubmed/20439717 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.1002762107 |
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