Showing results 9 to 11 of 11
Issue Date | Title | Journal Title |
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2022 | Precision Medicine through Next-Generation Sequencing in Inherited Eye Diseases in a Korean Cohort | GENES |
2020 | SLC38A8 mutations result in arrested retinal development with loss of cone photoreceptor specialization | HUMAN MOLECULAR GENETICS |
2021 | TUBB3 M323V Syndrome Presents with Infantile Nystagmus | GENES |