Researchers identify possible treatment for rare disorder CTNNB1 syndrome

Researchers identify possible treatment for rare disorder CTNNB1 syndrome

Researchers at Tufts University School of Medicine and the Graduate School of Biomedical Sciences (GSBS) have identified a small molecule that, in mouse and human cell models, rectifies the underlying molecular cause of a rare genetic developmental disorder linked with motor and intellectual disabilities and some types of autism spectrum disorder.

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