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. 2022 Oct 25;29(1):270–281. doi: 10.1111/cns.14001

FIGURE 1.

FIGURE 1

Genetic data on the patients with KCNH1 variants. (A, D) Pedigree of the two families. The filled symbol with arrows identifies the probands. (B, E) The variants c.338T>C and c.1069C>T were identified through whole‐exome sequencing and confirmed by Sanger sequencing. The SNVs were shown in gray shadows, c.338T>C was inherited from his mother, and c.1069C>T was de novo. (C, F) The variant amino acids in our patient were conserved from multiple species.