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...

Volledige beschrijving

Bewaard in:
Bibliografische gegevens
Hoofdauteurs: Aurora Alexandra Jurca, Alexandru Daniel Jurca, Codruta Diana Petchesi, Dan Bembea, Claudia Maria Jurca, Emilia Severin, Sanziana Jurca, Cosmin Mihai Vesa
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: MDPI AG 2025-02-01
Reeks:Life
Onderwerpen:
TSC1 gene
TSC2 gene
hamartomas
mTOR inhibitors
Online toegang:https://www.mdpi.com/2075-1729/15/3/368
Tags: Voeg label toe
Geen labels, Wees de eerste die dit record labelt!

Gelijkaardige items