6 results on '"Grinton BE"'
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2. Familial mesial temporal lobe epilepsy: a benign epilepsy syndrome showing complex inheritance
3. Temporal lobe epilepsy and GEFS+ phenotypes associated with SCN1B mutations
4. In vivo loss of slow potassium channel activity in individuals with benign familial neonatal epilepsy in remission
5. Familial mesial temporal lobe epilepsy: a benign epilepsy syndrome showing complex inheritance
6. Temporal lobe epilepsy and GEFS+ phenotypes associated with SCN1B mutations
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