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An affected core drives network integration deficits of the structural connectome in 22q11.2 deletion syndrome
Chromosome 22q11.2 deletion syndrome (22q11DS) is a genetic disease known to lead to cerebral structural alterations, which we study using the framework of the macroscopic white-matter connectome. We create weighted connectomes of 44 patients with 22q11DS and 44 healthy controls using diffusion tens...
में बचाया:
| में प्रकाशित: | Neuroimage Clin |
|---|---|
| मुख्य लेखकों: | , , , , , , |
| स्वरूप: | Artigo |
| भाषा: | Inglês |
| प्रकाशित: |
Elsevier
2015
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| विषय: | |
| ऑनलाइन पहुंच: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4711395/ https://ncbi.nlm.nih.gov/pubmed/26870660 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.nicl.2015.11.017 |
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