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1
S00439-017-1863-Y
S00439-017-1863-Y
http://dx.doi.org/10.1007/S00439-017-1863-Y
De novo variants in SETD1B are associated with intellectual disability, epilepsy and autism.
P356
Q50098318-EC81F476-78B5-4F59-8FA1-5079A8ADC724
P356
S00439-017-1863-Y
http://dx.doi.org/10.1007/S00439-017-1863-Y