Is Intrinsic Hyperexcitability in CA3 the Culprit for Seizures in Rett Syndrome?-Reference-Cited by-同舟云学术

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Is Intrinsic Hyperexcitability in CA3 the Culprit for Seizures in Rett Syndrome?

Published:2012-01 Issue:1 Volume:12 Page:13-14
ISSN:1535-7597
Container-title:Epilepsy Currents
language:en
Short-container-title:Epilepsy Curr

Author:

Boison Detlev

Publisher

SAGE Publications

Subject

Clinical Neurology

Link

http://journals.sagepub.com/doi/pdf/10.5698/1535-7511-12.1.13

Reference10 articles.

1. Review of Rett Syndrome

2. The Story of Rett Syndrome: From Clinic to Neurobiology

3. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2

4. Deficiency of methyl-CpG binding protein-2 in CNS neurons results in a Rett-like phenotype in mice

5. A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndrome

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Persistent Expression of Serotonin Receptor 5b Alters Breathing Behavior in Male MeCP2 Knockout Mice;Frontiers in Molecular Neuroscience;2018-02-20

2. Kappa opioid receptors regulate hippocampal synaptic homeostasis and epileptogenesis;Epilepsia;2017-11-08

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