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Tetrahydrobiopterin
Phenylalanine hydroxylase
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Key terms:
pku
phenylalanine
levels
acid
diet
amino acid
patients
gene
phenylketonuria
disorders
pah
mutated
normal
brain
mental
metabolic
tyrosine
foods
enzyme
screening
genetic
convert
phenylalanine hydroxylase
deficiency
pregnancy
parent
ranges
recessive
detection
accumulates
cofactor
autosomal recessive
elevated
allele
affected
incidence
seizure
newborn
high levels
dopamine
milk
monitored
clinical
babies
dominance
newborn screening
optimal
microcephaly
untreated
substance
neutral amino
diagnosed
physicians
brain development
Search external links cited by footnotes on Wikipedia page Phenylketonuria:
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