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Distinct phenotypes in zebrafish models of human startle disease()
Startle disease is an inherited neurological disorder that causes affected individuals to suffer noise- or touch-induced non-epileptic seizures, excessive muscle stiffness and neonatal apnea episodes. Mutations known to cause startle disease have been identified in glycine receptor subunit (GLRA1 an...
Tallennettuna:
| Päätekijät: | , , , , , , |
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| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Academic Press
2013
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3972633/ https://ncbi.nlm.nih.gov/pubmed/24029548 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.nbd.2013.09.002 |
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