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Mr. Dubey • 100.64K Points
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Q. PKU is one of the best-known hereditary disorders in amino acid metabolism. The defect is attributed to a lesion in one of the following enzymatic activities:

  • (A) Phenylalanine ammonia lyase
  • (B) Phenylalanine hydroxylase
  • (C) Tyrosine hydroxylase
  • (D) Phenylalanine transaminase
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