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Prevention of premature death and seizures in a Depdc5 mouse epilepsy model through inhibition of mTORC1
Mutations in DEP domain containing 5 (DEPDC5) are increasingly appreciated as one of the most common causes of inherited focal epilepsy. Epilepsies due to DEPDC5 mutations are often associated with brain malformations, tend to be drug-resistant, and have been linked to an increased risk of sudden un...
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| 出版年: | Hum Mol Genet |
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| 主要な著者: | , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Oxford University Press
2020
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7254848/ https://ncbi.nlm.nih.gov/pubmed/32280987 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddaa068 |
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