Journal of Genetic Medicine : eISSN 2383-8442 / pISSN 1226-1769

Fig. 3.

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Fig. 3. Sanger sequencing of the proband and her parents. Sequencing showed (A) a missense and (B) a nonsense mutation of the GRIN2A gene (c.1770A>C; p.Lys509Asn and c.3187G>T; p.Glu1063*, respectively).
Journal of Genetic Medicine 2020;17:79-82 https://doi.org/10.5734/JGM.2020.17.2.79
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