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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Autors principals: Romano, David, Nicolau, Monica, Quintin, Eve‐Marie, Mazaika, Paul K., Lightbody, Amy A., Cody Hazlett, Heather, Piven, Joseph, Carlsson, Gunnar, Reiss, Allan L.
Format: Artigo
Idioma:Inglês
Publicat: John Wiley and Sons Inc. 2014
Matèries:
Research Articles
Accés en línia: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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