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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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Bibliografski detalji
Glavni autori: Loat, C. S., Curran, S., Lewis, C. M., Duvall, J., Geschwind, D., Bolton, P., Craig, I. W.
Format: Artigo
Jezik:Inglês
Izdano: 2008
Teme:
Online pristup: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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