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Lifespan changes in working memory in fragile X premutation males
Fragile X syndrome is the world’s most common hereditary cause of developmental delay in males and is now well characterized at the biological, brain and cognitive levels. The disorder is caused by the silencing of a single gene on the X chromosome, the FMR1 gene. The premutation (carrier) status, h...
Gorde:
| Egile Nagusiak: | , , , , , |
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| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
2008
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| Gaiak: | |
| Sarrera elektronikoa: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4158922/ https://ncbi.nlm.nih.gov/pubmed/19114290 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.bandc.2008.11.006 |
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