(4792761), S. A., (17346976), J. A., (5125442), F. K., (612858), S. S., (14778937), R. H., (12040355), B. H., . . . (110443), K. H. (2019). A SLC16A1 Mutation in an Infant With Ketoacidosis and Neuroimaging Assessment: Expanding the Clinical Spectrum of MCT1 Deficiency.
توثيق أسلوب شيكاغو (الطبعة السابعة عشر)(4792761), Sara Al-Khawaga, Jehan AlRayahi (17346976), Faiyaz Khan (5125442), Saras Saraswathi (612858), Reem Hasnah (14778937), Basma Haris (12040355), Idris Mohammed (751020), Essam M. Abdelalim (5768072), و Khalid Hussain (110443). A SLC16A1 Mutation in an Infant With Ketoacidosis and Neuroimaging Assessment: Expanding the Clinical Spectrum of MCT1 Deficiency. 2019.
توثيق جمعية اللغة المعاصرة MLA (الإصدار التاسع)(4792761), Sara Al-Khawaga, et al. A SLC16A1 Mutation in an Infant With Ketoacidosis and Neuroimaging Assessment: Expanding the Clinical Spectrum of MCT1 Deficiency. 2019.