[Diagnosis and monitoring of phenylketonuria by LC-MS-MS in Morocco].
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DOI: 10.1684/abc.2021.1619
Abstract: Phenylketonuria is an inherited metabolic disease, of autosomal recessive transmission, due to the enzymatic deficit of phenylalanine hydroxylase, which transforms phenylalanine into tyrosine. The deficit leads to an increase in phenylalanine and its metabolite, phenylpyruvic… read more here.
Keywords: phenylketonuric patients; diagnosis monitoring; phenylalanine; morocco ... See more keywords