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Metabolism of Primed, Constant Infusions of [1,213c2] Glycine and [113c1] Phenylalanine to Urinary Oxalate
10.1111/j.1471-4159.2005.03618.x 115 SuS.LibmanR
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Patients who harbor mutations in selenoprotein synthesis show decreased levels of several selenoproteins and have characteristic abnormalities in thyroid hormone levels with high thyroxine T 4 and low triiodothyronine T 3 as well as short stature during childhood and bone maturation delay due to the decrease in selenoenzyme iodothyronine deiodinases
