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Distinct DNA binding and transcriptional repression characteristics related to different ARX mutations
Mutations in the Aristaless-related homeobox gene (ARX) are associated with a wide variety of neurologic disorders including lissencephaly, hydrocephaly, West syndrome, Partington syndrome, and X-linked intellectual disability with or without epilepsy. A genotype-phenotype correlation exists for ARX...
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| Main Authors: | , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2012
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3279587/ https://ncbi.nlm.nih.gov/pubmed/22252899 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s10048-011-0304-7 |
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