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

Fig. 3.

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Fig. 3. The novel missense variant, c.589A>6 (p.Asn197Asp), in the EBF3 gene of the patient (II:1). VUS, variants of uncertain significance.
Journal of Genetic Medicine 2020;17:92-6 https://doi.org/10.5734/JGM.2020.17.2.92
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