4-Chloropropofol enhances chloride currents in human hyperekplexic and artificial mutated glycine receptors
<p>Abstract</p> <p>Background</p> <p>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 c...
Main Authors: | , , , , , , |
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Format: | Article |
Language: | English |
Published: |
BMC
2012-09-01
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Series: | BMC Neurology |
Subjects: | |
Online Access: | http://www.biomedcentral.com/1471-2377/12/104 |