Publication | Closed Access
Significant correlation of the SCN1A mutations and severe myoclonic epilepsy in infancy
228
Citations
20
References
2002
Year
Scn1a MutationsSignificant CorrelationNeurological DisorderGeneticsGenetic DisorderNeuroscienceNeurologyCentral Nervous SystemNeuropathologyMedicineSevere Myoclonic EpilepsyNeurogenetics
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