A genetic variant that disrupts MET transcription is associated with autism
There is strong evidence for a genetic predisposition to autism and an intense interest in discovering heritable risk factors that disrupt gene function. Based on neurobiological findings and location within a chromosome 7q31 autism candidate gene region, we analyzed the gene encoding the pleiotropi...
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Main Authors: | , , , , , , , , , , , |
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Formato: | Artigo |
Idioma: | Inglês |
Publicado em: |
National Academy of Sciences
2006
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Assuntos: | |
Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1838551/ https://ncbi.nlm.nih.gov/pubmed/17053076 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.0605296103 |
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