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Scientists Find Genetic Cause, Underlying Mechanisms of New Neurodevelopmental Syndrome

July 1, 2021 sarah JonasResearch Results

UNC School of Medicine scientists have demonstrated that variants in the SPTBN1 gene can alter neuronal architecture, dramatically affecting their function and leading to a rare, newly defined neurodevelopmental syndrome in children.

A Key Player in Brain Development, Cell Communication Uncovered

June 25, 2021 sarah JonasResearch Results

For the first, time UNC School of Medicine scientist Katie Baldwin, PhD, and colleagues revealed a central role of the glial protein hepaCAM in building the brain and affecting brain function early in life.