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Sporadic Cone-Rod Dystrophy Caused by a Heterozygous RAB28 p.Ser23Phe Pathogenic Variant and a De Novo 4p16.1p15.33 Deletion

Research output: Contribution to journalJournal articlepeer-review

Original languageKorean
JournalBMC Medical Genomics
StatePublished - 2026.06.1

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