Alkaptonuria is due to the deficiency of
A. Phenylalanine hydroxylase
B. Homogentisate oxidase
C. β-N acetyl hexosaminidase
D. Galactose 1-phosphate uridyl transferase
Answer:B
Alkaptonuria is due to the deficiency of
A. Phenylalanine hydroxylase B. Homogentisate oxidase C. β-N acetyl hexosaminidase D. Galactose 1-phosphate uridyl transferase