Neuronal Nicotinic Acetylcholine Receptors and Epilepsy
The identification of a genetically transmissible form of epilepsy that is associated with a mutation in CHRNA4, the gene that encodes the α4 subunit of the high-affinity nicotinic acetylcholine receptor, was the first demonstration that an alteration in a ligand-gated ion channel can cause seizures...
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| Vydáno v: | Epilepsy Curr |
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| Hlavní autor: | |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
American Epilepsy Society
2002
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC321143/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/15309115/ https://ncbi.nlm.nih.govhttps://doi.org/10.1046/j.1535-7597.2002.00072.x |
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