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MeCP2 deficiency results in robust Rett-like behavioural and motor deficits in male and female rats
Since the identification of MECP2 as the causative gene in the majority of Rett Syndrome (RTT) cases, transgenic mouse models have played a critical role in our understanding of this disease. The use of additional mammalian RTT models offers the promise of further elucidating critical early mechanis...
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| Gepubliceerd in: | Hum Mol Genet |
|---|---|
| Hoofdauteurs: | , , , , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
Oxford University Press
2016
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5179928/ https://ncbi.nlm.nih.gov/pubmed/27329765 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddw179 |
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