Journal of Genetic Medicine : eISSN 2383-8442 / pISSN 1226-1769
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Seo E, Kim D, Hwang S, Koh J, Ju YS, Kim G, Lee BH.  Salih myopathy and Feingold syndrome type 1 caused by the <i>TTN</i> and <i>MYCN</i> mutation in an infant with congenital hypotonia.  J Genet Med 2024;21:74-79.  https://doi.org/10.5734/JGM.2024.21.2.74
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