Propofol Restores the Function of “Hyperekplexic” Mutant Glycine Receptors in Xenopus Oocytes and Mice

Human hereditary hyperekplexia (“startle disease”) is a neurological disorder characterized by exaggerated, convulsive movements in response to unexpected stimuli. Molecular genetic studies have shown that this disease is often caused by amino acid substitutions at arginine 271 to glutamine or leuci...

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Dettagli Bibliografici
Pubblicato in:J Neurosci
Autori principali: O'Shea, Sean Michael, Becker, Lore, Weiher, Hans, Betz, Heinrich, Laube, Bodo
Natura: Artigo
Lingua:Inglês
Pubblicazione: Society for Neuroscience 2004
Soggetti:
Brief Communications
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC6730415/
https://ncbi.nlm.nih.gov/pubmed/14999083
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1523/JNEUROSCI.4675-03.2004
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