Publication | Closed Access
A missense mutation in SCN1A in brothers with severe myoclonic epilepsy in infancy (SMEI) inherited from a father with febrile seizures
54
Citations
37
References
2005
Year
Mendelian DisorderGenetic DisorderGeneticsMissense MutationFebrile SeizuresMedicineSevere Myoclonic EpilepsyNeurogenetics
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