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Key terms: pku levels phenylalanine diet pah amino acid disorders patients brain risk mental enzyme tyrosine genetic phenylketonuria disease affected deficiency foods pku patients parent mutated cofactor pregnancy incidence phenylalanine levels autosomal recessive phenylalanine hydroxylase excessive low phenylalanine high levels dopamine milk monitored metabolic detected clinical screening babies classical pku dominance neutral amino therapy microcephaly untreated substance pah gene severe physicians accumulation Search external links cited by footnotes on Wikipedia page Phenylketonuria: |
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