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CCDS1, caused by genetic variants in the SLC6A8 gene, is an X-linked inherited metabolic disorder with common clinical manifestations including mental retardation, severe speech disorders, epilepsy, movement disorders, and behavioral disorders

Radioprotective effect of vitamin E on salivary glands after radioiodine therapy for differentiated thyroid cancer: a randomized-controlled trial

IsdG and IsdI, heme-degrading enzymes in the cytoplasm of Staphylococcus aureus

Underlying health conditions Those with cardiac issues, kidney problems, or other complex health conditions may also experience more severe interactions, as these individuals often have difficulties metabolizing both substances

Cell lines were fingerprinted by STR profiling to confirm identity and mycoplasma tested prior to use