Treating Rett syndrome: from mouse models to human therapies
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics
Link
http://link.springer.com/article/10.1007/s00335-019-09793-5/fulltext.html
Reference207 articles.
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3. Abdala AP, Toward MA, Dutschmann M et al (2016) Deficiency of GABAergic synaptic inhibition in the Kölliker-Fuse area underlies respiratory dysrhythmia in a mouse model of Rett syndrome. J Physiol 594:223–237. https://doi.org/10.1113/JP270966
4. Alpoz AR, Ergul N, Oncag O (1999) Bruxism in Rett syndrome: a case report. J Clin Pediatr Dent 23:161–163
5. Amaral MD, Pozzo-Miller L (2007) TRPC3 channels are necessary for brain-derived neurotrophic factor to activate a nonselective cationic current and to Induce dendritic spine formation. J Neurosci 27:5179–5189. https://doi.org/10.1523/JNEUROSCI.5499-06.2007
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