Showing results 1 to 2 of 2
Issue Date | Title | Journal Title |
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2021 | Eif2b3 mutants recapitulate phenotypes of vanishing white matter disease and validate novel disease alleles in zebrafish | HUMAN MOLECULAR GENETICS |
2020 | SLC38A8 mutations result in arrested retinal development with loss of cone photoreceptor specialization | HUMAN MOLECULAR GENETICS |