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2. Exon-disrupting deletions ofNRXN1in idiopathic generalized epilepsy

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3. Erratum: Exon-disrupting deletions of NRXN1 in idiopathic generalized epilepsy (Epilepsia (2013) 54 (256-264) DOI:10.1111/epi.12517)

4. Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1,2q22.3 and 17q21.32

5. Protocadherin 19 mutations in girls with infantile-onset epilepsy

7. Expansion of the first PolyA tract of ARX causes infantile spasms and status dystonicus

8. Expansion of the first PolyA tract of ARXcauses infantile spasms and status dystonicus