Al-Khawaga, S., Al-Khawaga, S., Al-Khawaga, S., AlRayahi, J., Khan, F., Saraswathi, S., . . . Hussain, K. (2019). A SLC16A1 Mutation in an Infant With Ketoacidosis and Neuroimaging Assessment: Expanding the Clinical Spectrum of MCT1 Deficiency. Frontiers Media S.A.
Chicago Style (17th ed.) CitationAl-Khawaga, Sara, et al. A SLC16A1 Mutation in an Infant With Ketoacidosis and Neuroimaging Assessment: Expanding the Clinical Spectrum of MCT1 Deficiency. Frontiers Media S.A, 2019.
MLA (8th ed.) CitationAl-Khawaga, Sara, et al. A SLC16A1 Mutation in an Infant With Ketoacidosis and Neuroimaging Assessment: Expanding the Clinical Spectrum of MCT1 Deficiency. Frontiers Media S.A, 2019.
Warning: These citations may not always be 100% accurate.