Corticospinal transmission to leg motoneurones in human subjects with deficient glycinergic inhibition
Normal coordinated movement requires that the activity of antagonistic motoneurones may be depressed at appropriate times during the movement. Both glycinergic and GABAergic inhibitory mechanisms participate in this control. Patients with the major form of hyperekplexia (hereditary startle disease)...
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Veröffentlicht in: | The Journal of physiology 2002-10, Vol.544 (2), p.631-640 |
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Sprache: | eng |
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