Labonne et al., 2016 - An atypical 12q24.31 microdeletion implicates six genes including a histone demethylase KDM2B and a histone methyltransferase SETD1B in syndromic intellectual disability. Human genetics   135(7):757-71 Full text @ Hum. Genet.
Human Disease / Model Data (1 Record)
Human Disease Fish Environment Evidence Code
syndromic intellectual disability
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