Sara Al-Khawaga, Sara Al-Khawaga, Sara Al-Khawaga, Jehan AlRayahi, Faiyaz Khan, Saras Saraswathi, . . . Khalid Hussain. (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.) CitationSara Al-Khawaga, 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 (9th ed.) CitationSara Al-Khawaga, 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.