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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Detalles Bibliográficos
Autores principales: Schubert-Bast, Susanne, Strzelczyk, Adam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2021
Materias:
Therapeutic Perspectives in Neurology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8290505/
https://www.ncbi.nlm.nih.gov/pubmed/34349839
http://dx.doi.org/10.1177/17562864211031100

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8290505/
https://www.ncbi.nlm.nih.gov/pubmed/34349839
http://dx.doi.org/10.1177/17562864211031100

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