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Breathing dysfunctions associated with impaired control of postinspiratory activity in Mecp2(−/y) knockout mice
Rett syndrome (RTT) is an inborn neurodevelopmental disorder caused by mutations in the X-linked methyl-CpG binding protein 2 gene (MECP2). Besides mental retardation, most patients suffer from potentially life-threatening breathing arrhythmia. To study its pathophysiology, we performed comparative...
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| Hlavní autoři: | , , , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Blackwell Science Inc
2007
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2151368/ https://ncbi.nlm.nih.gov/pubmed/17204503 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1113/jphysiol.2006.119966 |
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