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NN.4169
NN.4169
http://dx.doi.org/10.1038/NN.4169
Mutations in NONO lead to syndromic intellectual disability and inhibitory synaptic defects
P356
Q30845425-B393F680-CD7C-40F3-95A6-6F631B97469D
P356
NN.4169
http://dx.doi.org/10.1038/NN.4169