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. 2017 Mar 14;88(11):1037–1044. doi: 10.1212/WNL.0000000000003716

Figure 2. Pedigrees of families exhibiting incomplete penetrance of SCN1A mutations.

Figure 2

Inline graphic = Dravet syndrome; Inline graphic = FS; Inline graphic = generalized/genetic epilepsy with febrile seizures plus; Inline graphic = focal epilepsy; +/− = heterozygous SCN1A mutation; +/+ = absence of the SCN1A mutation.