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Paper Details

De novo mutations in epileptic encephalopathies.
Nature
1102
2013
ALG13, CACNA1A, CHD2, Epileptic encephalopathies, FLNA, GABRA1, GABRB3, GRIN1, GRIN2B, HNRNPU, IQSEC2, Lennox-Gastaut syndrome, MTOR, NEDD4L, autism spectrum disorders, childhood epilepsy disorders, epileptic encephalopathies, epileptic encephalopathy, exomes, fragile X, fragile X protein, gene sets, human, infantile spasms, patients

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