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Molecular Basis for and chemogenetic Rescue of Comorbidities in GABRG2-Deficient Epilepsies
SUMMARY: OBJECTIVE: GABA(A) receptor subunit gene mutations are significant causes of epilepsy, which are often accompanied with various neuropsychiatric comorbidities, but the underlying mechanisms are unclear. It has been suggested that the comorbidities are caused by seizures as they often presen...
Tallennettuna:
| Julkaisussa: | Epilepsia |
|---|---|
| Päätekijät: | , , , , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
2019
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6880653/ https://ncbi.nlm.nih.gov/pubmed/31087664 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/epi.15160 |
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