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. Author manuscript; available in PMC: 2020 Dec 1.
Published in final edited form as: Epilepsia. 2019 Dec;60(Suppl 3):S86–S91. doi: 10.1111/epi.14703

Figure 1.

Figure 1.

SCN8A mutations associated with epileptic encephalopathy. The protein structure of the four-domain sodium channel Nav1.6 is represented; each symbol represents a patient mutation. The positions of the two mutations studied in mouse models are indicated with arrows.