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Biochemistry Proteins and Amino Acids da0a0123

Enzyme deficiency in Alkaptonuria is

A
Tyrosine hydroxylase
B
Homogentisate acid oxidase
C
Phenyl alanine hydroxylase
D
Cystathione synthase
High-Yield Explanation
B. i.e. (Homogentisate oxidase) (259 - Harper 27th)ALKAPTONURIA = lack of enzyme homogentisate oxidase enzyme most striking clinical manifestation - occurrence of dark urine black on standing in air*** Classical type Galactosemia - Galactose-1 p- uridyl transferase enzyme* Classical phenylketonuria - Phenyl alanine hydroxylase* Type I Tyrosinemia - Fumatyl acetoacetate hydrolase enzyme* Type II Tyrosinemia - Hepatic transaminase enzyme.

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