4-Chloropropofol enhances chloride currents in human hyperekplexic and artificial mutated glycine receptors

Author:

de la Roche Jeanne,Leuwer Martin,Krampfl Klaus,Haeseler Gertrud,Dengler Reinhard,Buchholz Vanessa,Ahrens Jörg

Publisher

Springer Science and Business Media LLC

Subject

Neurology (clinical),General Medicine

Reference49 articles.

1. Harvey RJ, Topf M, Harvey K, Rees MI: The genetics of hyperekplexia: more than startle!. Trends Genet. 2008, 24 (9): 439-447. 10.1016/j.tig.2008.06.005.

2. Praveen V, Patole SK, Whitehall JS: Hyperekplexia in neonates. Postgraduate Medical Journal. 2001, 77 (911): 570-572. 10.1136/pmj.77.911.570.

3. Ryan SG, Dixon MJ, Nigro MA, Kelts KA, Markand ON, Terry JC, Shiang R, Wasmuth JJ, O'Connell P: Genetic and radiation hybrid mapping of the hyperekplexia region on chromosome 5q. AmJHumGenet. 1992, 51 (6): 1334-1343.

4. Andermann F, Keene DL, Andermann E, Quesney LF: Startle disease or hyperekplexia: further delineation of the syndrome. Brain. 1980, 103 (4): 985-997. 10.1093/brain/103.4.985.

5. Davies JS, Chung SK, Thomas RH, Robinson A, Hammond CL, Mullins JG, Carta E, Pearce BR, Harvey K, Harvey RJ, et al: The glycinergic system in human startle disease: a genetic screening approach. Front Mol Neurosci. 2010, 3 (8): 10-

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