Tuberous Sclerosis Complex: New Insights into Pathogenesis and Therapeutic Breakthroughs

<b>Background/Objectives</b>: Tuberous sclerosis complex (TSC) is a rare, autosomal dominant genetic disorder caused by mutations in the <i>TSC1</i> and <i>TSC2</i> genes, which disrupt the regulation of the mammalian target of rapamycin (mTOR) pathway, a critical...

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Main Authors: Aurora Alexandra Jurca, Alexandru Daniel Jurca, Codruta Diana Petchesi, Dan Bembea, Claudia Maria Jurca, Emilia Severin, Sanziana Jurca, Cosmin Mihai Vesa
Formato: Artigo
Idioma:Inglês
Publicado: MDPI AG 2025-02-01
Series:Life
Assuntos:
TSC1 gene
TSC2 gene
hamartomas
mTOR inhibitors
Acceso en liña:https://www.mdpi.com/2075-1729/15/3/368
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