Стиль цитування APA (7-ме видання)

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..

Чикаго стиль цитування (17-те видання)

Sara 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.

Стиль цитування MLA (9-ме видання)

Sara 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.