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Age-dependent expression of MeCP2 in a heterozygous mosaic mouse model
Functional deficiency of the X-linked methyl-CPG binding protein 2 (MeCP2) leads to the neurodevelopmental disorder Rett syndrome (RTT). Due to random X-chromosome inactivation (XCI), most RTT patients are females who are heterozygous for the MECP2 mutation and therefore mosaic in MeCP2 deficiency....
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| Päätekijät: | , , |
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| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Oxford University Press
2011
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3071674/ https://ncbi.nlm.nih.gov/pubmed/21330301 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddr066 |
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