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Frontostriatal deficits in fragile X syndrome: Relation to FMR1 gene expression
Fragile X syndrome (fraX) is the most common known cause of inherited developmental disability. fraX is associated with a CGG expansion in the FMR1 gene on the long arm of the X chromosome. Behavioral deficits, including problems with impulse control and distractibility, are common in fraX. We used...
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| Main Authors: | , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
National Academy of Sciences
2004
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| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC373511/ https://ncbi.nlm.nih.gov/pubmed/14993603 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.0304544101 |
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