Transient neuromotor phenotype in transgenic spastic mice expressing low levels of glycine receptor β‐subunit: an animal model of startle disease
Startle disease or hereditary hyperekplexia has been shown to result from mutations in the α1‐subunit gene of the inhibitory glycine receptor (GlyR). In hyperekplexia patients, neuromotor symptoms ge...
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| Main Authors: | , , , , , |
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| Format: | Article (Journal) |
| Language: | English |
| Published: |
2000
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| In: |
European journal of neuroscience
Year: 2000, Volume: 12, Issue: 1, Pages: 27-32 |
| ISSN: | 1460-9568 |
| DOI: | 10.1046/j.1460-9568.2000.00877.x |
| Online Access: | Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1046/j.1460-9568.2000.00877.x Verlag, lizenzpflichtig, Volltext: https://onlinelibrary.wiley.com/doi/10.1046/j.1460-9568.2000.00877.x 
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| Author Notes: | Lore Becker, Bettina Hartenstein, Johannes Schenkel, Jochen Kuhse, Heinrich Betz and Hans Weiher |
| Summary: | Startle disease or hereditary hyperekplexia has been shown to result from mutations in the α1‐subunit gene of the inhibitory glycine receptor (GlyR). In hyperekplexia patients, neuromotor symptoms ge... |
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| Item Description: | Published: 09 October 2008 Elektronische Reproduktion der Druck-Ausgabe Gesehen am 10.05.2021 |
| Physical Description: | Online Resource |
| ISSN: | 1460-9568 |
| DOI: | 10.1046/j.1460-9568.2000.00877.x |