APA (7th ed.) Citation

Ng, B. G., Eklund, E. A., Rosenfeld, J. A., Elias, A. F., Abu-El-Haija, A., Bris, C., . . . Okur, V. Autosomal dominant HK1-related neurodevelopmental disorder with visual defects and brain anomalies (NEDVIBA): An emerging mitochondrial disorder. Elsevier.

Chicago Style (17th ed.) Citation

Ng, Bobby G., et al. Autosomal Dominant HK1-related Neurodevelopmental Disorder with Visual Defects and Brain Anomalies (NEDVIBA): An Emerging Mitochondrial Disorder. Elsevier.

MLA (9th ed.) Citation

Ng, Bobby G., et al. Autosomal Dominant HK1-related Neurodevelopmental Disorder with Visual Defects and Brain Anomalies (NEDVIBA): An Emerging Mitochondrial Disorder. Elsevier.