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Determination of SCN1A genetic variants in Mexican patients with refractory epilepsy and Dravet syndrome.

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Figure

Figure 1. Electropherogram showing the mutation c.5324 T>C (L1775P). Reverse primer, wild allele: A; Forward primer, wild allele: T.
Figure 2. PolyPhen-2 analysis showing the probability of the mutation c.5324 T>C being damaging.

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