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From neurodevelopment to neurodegeneration: utilizing human stem cell models to gain insight into Down syndrome

Down syndrome (DS), caused by triplication of chromosome 21, is the most frequent aneuploidy observed in the human population and represents the most common genetic form of intellectual disability and early-onset Alzheimer’s disease (AD). Individuals with DS exhibit a wide spectrum of clinical prese...

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Bibliográfalaš dieđut
Váldodahkkit: L. Ashley Watson, Hiruy S. Meharena
Materiálatiipa: Artigo
Giella:Inglês
Almmustuhtton: Frontiers Media S.A. 2023-05-01
Ráidu:Frontiers in Genetics
Fáttát:
Liŋkkat:https://www.frontiersin.org/articles/10.3389/fgene.2023.1198129/full
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