DOI:
10.1055/s-00000004
Aktuelle Neurologie
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References
Veeramah KR, O’Brien JE, Meisler MH et al.
De novo pathogenic SCN8A mutation identified by whole-genome sequencing of a family quartet affected by infantile epileptic encephalopathy and SUDEP.
Am J Hum Genet 2012;
90: 502-510
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