APA (7th ed.) Citation

BG, N., EA, E., JA, R., AF, E., A, A., C, B., . . . V, O. (2025). Autosomal dominant HK1-related neurodevelopmental disorder with visual defects and brain anomalies (NEDVIBA): An emerging mitochondrial disorder. Genetics in medicine open, 3, 103425. https://doi.org/10.1016/j.gimo.2025.103425

Chicago Style (17th ed.) Citation

BG, Ng, et al. "Autosomal Dominant HK1-related Neurodevelopmental Disorder with Visual Defects and Brain Anomalies (NEDVIBA): An Emerging Mitochondrial Disorder." Genetics in Medicine Open 3 (2025): 103425. https://doi.org/10.1016/j.gimo.2025.103425.

MLA (9th ed.) Citation

BG, Ng, et al. "Autosomal Dominant HK1-related Neurodevelopmental Disorder with Visual Defects and Brain Anomalies (NEDVIBA): An Emerging Mitochondrial Disorder." Genetics in Medicine Open, vol. 3, 2025, p. 103425, https://doi.org/10.1016/j.gimo.2025.103425.