Longitudinal identification of clinically distinct neurophenotypes in young children with fragile X syndrome

Fragile X syndrome (FXS), due to mutations of the FMR1 gene, is the most common known inherited cause of developmental disability. The cognitive, behavioral, and neurological phenotypes observed in affected individuals can vary considerably, making it difficult to predict outcomes and determine the...

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Shranjeno v:
Bibliografske podrobnosti
izdano v:Proc Natl Acad Sci U S A
Main Authors: Bruno, Jennifer L., Romano, David, Mazaika, Paul, Lightbody, Amy A., Hazlett, Heather Cody, Piven, Joseph, Reiss, Allan L.
Format: Artigo
Jezik:Inglês
Izdano: National Academy of Sciences 2017
Teme:
Biological Sciences
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC5635864/
https://ncbi.nlm.nih.gov/pubmed/28923933
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.1620994114
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