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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 α(1)-subunit gene of the inhibitory glycine receptor (GlyR). In hyperekplexia patients, neuromotor symptoms generally become apparent at birth, improve with age, and often disappear in adulthood. Loss-of-funct...
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| Hauptverfasser: | , , , , , |
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| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
Blackwell Science Ltd
2000
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3655541/ https://ncbi.nlm.nih.gov/pubmed/10651857 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1046/j.1460-9568.2000.00877.x |
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