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Methyl-CpG-binding protein 2 polymorphisms and vulnerability to autism
The methyl-binding protein gene, MECP2, is a candidate for involvement in autism through its implication as a major causative factor in Rett syndrome that has similarities to autism. Rare mutations in MECP2 have also been identified in autistic individuals. We have examined the possible broader invo...
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| Autors principals: | , , , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2008
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3645848/ https://ncbi.nlm.nih.gov/pubmed/19125863 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1601-183X.2008.00414.x |
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