PKU is a congenital amino acid metabolic disorder. In the following rare variants of PKU, dihydrobiopterin synthesis is affected. The enzyme deficient is

Correct Answer: Dihydropterin reductase
Description: In Type 2 and 3 of PKU, there is deficiency of enzyme dihydrobiopterin reductase. Hence there is deficiency of dihydrobiopterin.Ref: DM Vasudevan - Textbook of Biochemistry, 7th edition, page no: 236
Category: Biochemistry
Share:

Get More
Subject Mock Tests

Practice with over 200,000 questions from various medical subjects and improve your knowledge.

Attempt a mock test now
Mock Exam

Take an exam with 100 random questions selected from all subjects to test your knowledge.

Coming Soon
Get More
Subject Mock Tests

Try practicing mock tests with over 200,000 questions from various medical subjects.

Attempt a mock test now
Mock Exam

Attempt an exam of 100 questions randomly chosen from all subjects.

Coming Soon
WordPress › Error

There has been a critical error on this website.

Learn more about troubleshooting WordPress.