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Topological methods reveal high and low functioning neuro‐phenotypes within fragile X syndrome
Fragile X syndrome (FXS), due to mutations of the FMR1 gene, is the most common known inherited cause of developmental disability as well as the most common single‐gene risk factor for autism. Our goal was to examine variation in brain structure in FXS with topological data analysis (TDA), and to as...
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| Main Authors: | , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
John Wiley and Sons Inc.
2014
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4113391/ https://ncbi.nlm.nih.gov/pubmed/24737721 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/hbm.22521 |
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