DOI:
10.1055/s-00029030
Journal of Pediatric Neurology
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References
Touma M, Joshi M, Connolly MC. et al.
Whole genome sequencing identifies SCN2A mutation in monozygotic twins with Ohtahara syndrome and unique neuropathologic findings.
Epilepsia 2013;
54 (05) e81-e85
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