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Review of targeted treatments in fragile X syndrome
Fragile X syndrome (FXS) is the most common inherited form of intellectual disability, and is the leading single-gene cause of autism spectrum disorders. It is due to a loss of the fragile X mental retardation protein, which leads to molecular, behavioral, and cognitive deficits in these patients. I...
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| Publicado no: | Intractable Rare Dis Res |
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| Main Authors: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
International Research and Cooperation Association for Bio & Socio-Sciences Advancement
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4995416/ https://ncbi.nlm.nih.gov/pubmed/27672538 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5582/irdr.2016.01045 |
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