Search Results - Yong Gon Cho

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    Case Report: Novel Likely Pathogenic ACTN2 Variant Causing Heterogeneous Phenotype in a Korean Family With Left Ventricular Non-compaction by Joonhong Park, Joonhong Park, Yong Gon Cho, Yong Gon Cho, Ha Wook Park, Jung Sun Cho

    Published 2021
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    Case report: Compound heterozygosity in PKLR gene with a large exon deletion and a novel rare p.Gly536Asp variant as a cause of severe pyruvate kinase deficiency by Minsun Kim, Seung Yeob Lee, Seung Yeob Lee, Namsu Kim, Namsu Kim, Jaehyeon Lee, Jaehyeon Lee, Dal Sik Kim, Dal Sik Kim, Joonhong Park, Joonhong Park, Yong Gon Cho, Yong Gon Cho

    Published 2022
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