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Absence of association between a polymorphic GGC repeat in the 5' untranslated region of the reelin gene and autism
Autism is a complex neurodevelopmental disorder with severe cognitive and communication disabilities, that has a strong genetic predisposition predisposition.1 Reelin, a protein involved in neuronal migration during development, is encoded by a gene located on 7q22, 7q22,2 within the candidate regio...
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| Main Authors: | , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Nature Publishing Group Specialist Journals
2002
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1913931/ https://ncbi.nlm.nih.gov/pubmed/12192627 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/sj.mp.4001071 |
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