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Biochemistry Metabolism of protein and amino acid e141dac6

Phenylketonuria is caused by deficiency of

A
Tyrosine transminase
B
Tyrosine hydroxylase
C
Phenylalanine transaminase
D
Phenylalanine hydroxylase
High-Yield Explanation
Deficiency of Phenylalanine hydroxylase is the cause of PKU. The genetic mutation may be in such a way that either the enzyme is not synthesized or a non-functional enzyme is synthesized.Ref: DM Vasudevan - Textbook of Biochemistry, 7th edition, page no: 236

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