S-EPMC12135434 - Autosomal dominant HK1-related neurodevelopmental disorder with visual defects and brain anomalies (NEDVIBA): An emerging mitochondrial disorder - OmicsDI

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Autosomal dominant HK1-related neurodevelopmental disorder with visual defects and brain anomalies (NEDVIBA): An emerging mitochondrial disorder

ABSTRACT:

SUBMITTER: Ng B

PROVIDER: S-EPMC12135434 | biostudies-literature | 2025 Jan

REPOSITORIES: biostudies-literature