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4-Chloropropofol enhances chloride currents in human hyperekplexic and artificial mutated glycine receptors
BACKGROUND: The mammalian neurological disorder hereditary hyperekplexia can be attributed to various mutations of strychnine sensitive glycine receptors. The clinical symptoms of “startle disease” predominantly occur in the newborn leading to convulsive hypertonia and an exaggerated startle respons...
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| Autors principals: | , , , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
BioMed Central
2012
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3517478/ https://ncbi.nlm.nih.gov/pubmed/23006332 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2377-12-104 |
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