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Modeling Pathogenesis and Treatment Response in Childhood Absence Epilepsy
OBJECTIVE: Childhood Absence Epilepsy (CAE) is a genetic generalized epilepsy syndrome with polygenic inheritance, with genes for GABA receptors and T-type calcium channels implicated in the disorder. Previous studies of T-type calcium channel electrophysiology have shown genetic changes and medicat...
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| Vydáno v: | Epilepsia |
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| Hlavní autoři: | , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
2017
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5776688/ https://ncbi.nlm.nih.gov/pubmed/29265352 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/epi.13962 |
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