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Inhibition Deficits are Modulated by Age and CGG Repeat Length in Carriers of the FMR1 Premutation Allele who are Mothers of Children with Fragile X Syndrome
Individuals who carry a premutation (PM) allele on the FMR1 gene may experience executive limitations associated with their genetic status, including inhibition deficits. However, poor understanding of individualized risk factors has limited clinical management of this group, particularly in mothers...
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| Publicado no: | Brain Cogn |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6954879/ https://ncbi.nlm.nih.gov/pubmed/31887710 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.bandc.2019.105511 |
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