Which enzyme deficiency is associated with the development of Phenylketonuria, a genetic disorder characterized by an inability to break down the amino acid phenylalanine?

A Phenylalanine Hydroxylase
B Tyrosinase
C Homogentisate 1,2-Dioxygenase
D Cystathionine Beta-Synthase
Phenylalanine Hydroxylase is the enzyme responsible for converting phenylalanine into tyrosine. A deficiency in this enzyme leads to the accumulation of phenylalanine, causing Phenylketonuria.
NCERT Class 12 Biochemistry
Enzymes in Disease Biochemistry Amino Acid Metabolism Disorders Medium MEDICAL Confidence: high