Possible involvement of a gamma-hydroxybutyric acid receptor in startle disease
Author:
Publisher
Wiley
Subject
General Medicine,Pediatrics, Perinatology, and Child Health
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1651-2227.1994.tb13113.x/fullpdf
Reference15 articles.
1. Hyperexplcxia or stiff baby syndrome;Tohier;Arch Dis Child,1991
2. Hereditary stiff-baby syndrome;Lingam;Am J Dis Child,1981
3. Startle disease, or hyperexplexia response to clonazepam and assignment of the gene (STHE) to chromosome 5q by linkage analysis;Ryan;Ann Neurol,1992
4. Low cerebrospinal fluid concentration of free gamma-aminobutyric acid in startle disease;Dubowitz;Lancet,1992
5. Vigabatrin for startle-disease with altered cerebrospinal-fluid free gamma-aminobutyric acid;Stephenson;Lancet,1992
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