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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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| Pubblicato in: | Proc Natl Acad Sci U S A |
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| Autori principali: | , , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
National Academy of Sciences
2017
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| Soggetti: | |
| Accesso online: | 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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