[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 http://www.nature.com/nm/journal/v21/n12/full/nm.3982.html Collaboration with Joseph G. Gleeson (UCSD)
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