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Review of the treatment options for epilepsy in tuberous sclerosis complex: towards precision medicine
Tuberous sclerosis complex (TSC) is a rare genetic disorder caused by mutations in the TSC1 or TSC2 genes, which encode proteins that antagonise the mammalian isoform of the target of rapamycin complex 1 (mTORC1) – a key mediator of cell growth and metabolism. TSC is characterised by the development...
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| Udgivet i: | Ther Adv Neurol Disord |
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| Main Authors: | , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
SAGE Publications
2021
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8290505/ https://ncbi.nlm.nih.gov/pubmed/34349839 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/17562864211031100 |
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