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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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| Publicado en: | Ther Adv Neurol Disord |
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| Autores principales: | , |
| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
SAGE Publications
2021
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| Materias: | |
| Acceso en línea: | 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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