QT c interval and ventricular action potential prolongation in the Mecp2 Null/ + murine model of Rett syndrome
Author:
Affiliation:
1. School of Physiology, Pharmacology and Neuroscience University Walk Bristol UK
Publisher
Wiley
Subject
Physiology (medical),Physiology
Link
https://onlinelibrary.wiley.com/doi/pdf/10.14814/phy2.15437
Reference44 articles.
1. Effect of Sarizotan, a 5-HT1aand D2-Like Receptor Agonist, on Respiration in Three Mouse Models of Rett Syndrome
2. Abdala SheikhAP.Algorhythms for the analysis of unrestrained whole‐body plethysmography in mice. Figshare. Figshare Softwarehttps://doi.org/10.6084/m9.figshare.19518877.v2.2022.
3. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2
4. MECP2 mutations account for most cases of typical forms of Rett syndrome
5. Deficiency of methyl-CpG binding protein-2 in CNS neurons results in a Rett-like phenotype in mice
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