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Breathing dysfunction in Rett syndrome: Understanding epigenetic regulation of the respiratory network
Severely arrhythmic breathing is a hallmark of Rett syndrome (RTT) and profoundly affects quality of life for patients and their families. The last decade has seen the identification of the disease-causing gene, methyl-CpG-binding protein 2 (Mecp2) and the development of mouse models that phenocopy...
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| Hlavní autoři: | , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
2008
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2664709/ https://ncbi.nlm.nih.gov/pubmed/18534925 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.resp.2008.04.005 |
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