DOI:
10.1055/s-00029025
Journal of Pediatric Epilepsy
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References
Suls A, Claeys KG, Goossens D , et al.
Microdeletions involving the SCN1A gene may be common in SCN1A-mutation-negative SMEI patients.
Hum Mutat 2006;
27 (9) 914-920
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