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ELIFE.32451
ELIFE.32451
http://dx.doi.org/10.7554/ELIFE.32451
A homozygous loss-of-function CAMK2A mutation causes growth delay, frequent seizures and severe intellectual disability.
P356
Q54963859-661D1276-45BF-4C01-B728-4847D62F2DBF
P356
ELIFE.32451
http://dx.doi.org/10.7554/ELIFE.32451