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YUHSpace1. College of Medicine (의과대학)Dept. of Laboratory Medicine (진단검사의학교실)1. Journal Papers

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Issue DateTitleJournal Title
2021Eif2b3 mutants recapitulate phenotypes of vanishing white matter disease and validate novel disease alleles in zebrafishHUMAN MOLECULAR GENETICS
2020SLC38A8 mutations result in arrested retinal development with loss of cone photoreceptor specialization HUMAN MOLECULAR GENETICS
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