Population
A 4-generational Bulgarian family with an epileptic disorder characterized by febrile and afebrile…
Design
Case_series
Authors
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Inherited SCN1A deletions may underlie variable familial epilepsy beyond Dravet; extends spectrum but leaves broader implications open from single case.
An inherited SCN1A gene deletion can cause significant intrafamilial clinical variability and is not exclusively associated with Dravet syndrome.
Suls et al. (2010) studied this question.
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