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Chunk #28 — 5. Induced-pluripotent stem cell models of neurodevelopmental disease — a. Penetrant mutations

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Human induced pluripotent stem cells for modelling neurodevelopmental disorders.
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The most extensive work in hiPSC modeling of neurodevelopmental disorders has been done in the context of the monogenic disorder, Rett Syndrome (RTT). However, Fragile X syndrome (FXS) and Timothy syndrome (TS) are other monogenic neurodevelopmental disorders that have been studied with hiPSC models; the symptoms of both of these disorders include symptoms of autism spectrum disorder (ASD).