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PAH encodes the enzyme phenylalanine hydroxylase that is the rate-limiting step in phenylalanine catabolism. Deficiency of this enzyme activity results in the autosomal recessive disorder phenylketonuria.
AW106920; Pah; PH; phe-4-monooxygenase; phenylalanine 4-monooxygenase; phenylalanine hydroxylase; phenylalanine-4-hydroxylase; PKU; PKU1
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100 µg
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400 µL
50 µg
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