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Biochemistry General d4a9513b

Hyperammonemia type-1 is due to deficiency of

A
Arginase
B
Arginosuccinate lyase
C
Arginosuccinate synthase
D
CPS-1
High-Yield Explanation
Ans. is 'd' i.e., CPS-1 Disorders caused by genetic defects of urea cycle enzymesHyperammonemia type-I Hyperammonemia type-II Citrullinemia Argininosuccinic aciduria Argi ninemiaDefective enzymeCarbamoyl phosphate synthase-I Ornithine transcarbamoylase Argininosuccinate synthase Argininosuccinate lyase ArginaseProducts accumulatedAmmonia Ammonia Citrulline Argininosuccinate Arginine.

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