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. 2024 Dec 17;11(1):e200223. doi: 10.1212/NXG.0000000000200223

Figure 3. Pedigree.

Figure 3

The patient inherited a pathogenic variant in the CLCN1 gene from his asymptomatic father and a variant of uncertain significance in the SCN4A gene from his mother, who has milder clinical and electrographic myotonia. The patient's brother, niece, and nephew are unaffected.