APA (7th ed.) Citation

Alotaibi, M., Alqasmi, A., Albassam, F., Alkahtani, T., Alqahtany, M., & Alkhaldi, M. The First Reported Case of a Child with Two Different Rare Metabolic Disorders: Very Long-Chain Acyl-CoA Dehydrogenase Deficiency and Encephalomyopathic Mitochondrial DNA Depletion Syndrome 13. KeAi Communications Co., Ltd.

Chicago Style (17th ed.) Citation

Alotaibi, Maha, Amal Alqasmi, Faisal Albassam, Turki Alkahtani, Muath Alqahtany, and Mohammed Alkhaldi. The First Reported Case of a Child with Two Different Rare Metabolic Disorders: Very Long-Chain Acyl-CoA Dehydrogenase Deficiency and Encephalomyopathic Mitochondrial DNA Depletion Syndrome 13. KeAi Communications Co., Ltd.

MLA (9th ed.) Citation

Alotaibi, Maha, et al. The First Reported Case of a Child with Two Different Rare Metabolic Disorders: Very Long-Chain Acyl-CoA Dehydrogenase Deficiency and Encephalomyopathic Mitochondrial DNA Depletion Syndrome 13. KeAi Communications Co., Ltd.