Cargando…
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...
| Autores principales: | , , , , , |
|---|---|
| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Blackwell Science Ltd
2000
|
| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3655541/ https://www.ncbi.nlm.nih.gov/pubmed/10651857 http://dx.doi.org/10.1046/j.1460-9568.2000.00877.x |