Browsing by Subject "Phenylalanine hydroxylase (PAH), Phenylalaninase, PKU, PKU1."
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Phenylketonuria: Genes in phenylketonuria, diagnosis, and treatments
(African Journal of Biological Sciences, 2020-01-01)Introduction: Phenylketonuria (PKU) is a rare autosomal-recessive disorder inherited in accordance with the law of segregation. Detection tools for people with PKU can include Sanger Sequencing (SS) and Next Generation ...