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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Huvudupphovsmän: Cho, Ginam, Nasrallah, MacLean P., Lim, Youngshin, Golden, Jeffrey A
Materialtyp: Artigo
Språk:Inglês
Publicerad: 2012
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Article
Länkar: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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