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Objective
Focal cortical dysplasia type II (FCDII) is a malformation of cortex development commonly found in children with drug‐resistant epilepsy. FCDII has been associated with somatic mutations in mammalian target of rapamycin (mTOR)‐related pathway genes and an upregulation of mTOR. Somatic mutations were found in 10%‐63% of FCDII samples; the frequency of the mutant allele was 0.93%‐33.5%. This...
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