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

    Authors: Ng BG Eklund EA Rosenfeld JA et al.

    Source: Genetics in medicine open [Genet Med Open] 2025 Mar 20; Vol. 3, pp. 103425. Date of Electronic Publication: 2025 Mar 20 (Print Publication: 2025).

    Publication Type: Journal Article

    Journal Info: Publisher: Elsevier Inc Country of Publication: United States NLM ID: 9918734281906676 Publication Model: eCollection Cited Medium: Internet ISSN: 2949-7744 (Electronic) Linking ISSN: 29497744 NLM ISO Abbreviation: Genet Med Open Subsets: PubMed not MEDLINE

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