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[New paper] The mechanism in which AKT3 pathway causes cortical malformation

A new paper published in Nature Medicine

In this study, Sangwoo Kim joined to identify how abnormal AKT3 pathway activation causes malformation of cortical development.

An AKT3-FOXG1-reelin network underlies defective migration in human focal malformations of cortical development Collaboration with Joseph G. Gleeson (UCSD)

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