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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...

पूर्ण विवरण

में बचाया:
ग्रंथसूची विवरण
में प्रकाशित:Ther Adv Neurol Disord
मुख्य लेखकों: Schubert-Bast, Susanne, Strzelczyk, Adam
स्वरूप: Artigo
भाषा:Inglês
प्रकाशित: SAGE Publications 2021
विषय:
ऑनलाइन पहुंच: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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