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FNMOL.2018.00269
FNMOL.2018.00269
http://dx.doi.org/10.3389/FNMOL.2018.00269
A Loss-of-Function Mutation Associated With Familial Benign Myoclonic Epilepsy in Infancy Causes Increased Neuronal Excitability
P356
Q58798982-E2905BAB-3370-4433-80DA-9F457F2C628B
P356
FNMOL.2018.00269
http://dx.doi.org/10.3389/FNMOL.2018.00269