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[Individuals, with hypermethioninemia due to one of the MAT1A mutations that in heterozygotes cause relatively mild and clinically benign hypermethioninemia are currently often being flagged in screening programs measuring methionine elevation to identify newborns with defective cystathionine ?-synthase activity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
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