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Molecular and Cellular Mechanisms of Learning Disabilities: A Focus on NF1
Neurofibromatosis Type I (NF1) is a single-gene disorder characterized by a high incidence of complex cognitive symptoms, including learning disabilities, attention deficit disorder, executive function deficits, and motor coordination problems. Since the underlying genetic cause of this disorder is...
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| Main Authors: | , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2010
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3063104/ https://ncbi.nlm.nih.gov/pubmed/20345245 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1146/annurev-neuro-060909-153215 |
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