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BIOCHEMISTRY BOOKS ALC&MOD MST/ET PKG
1st Edition
ISBN: 9780134172507
Author: APPLING
Publisher: Pearson Education
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Chapter 18, Problem 18P
Interpretation Introduction
Interpretation:
Sketch the curve predicting the concentration of phenylalanine versus time displayed by an affected individual, a heterozygote, and a normal individual.
How one can distinguish between PKU resulting from Phenylalanine hydroxylase deficiency or dihydropteridine reductase deficiency.
Concept Introduction:
The phenylketonuria is an autosomal recessive disorder. In the phenylketonuria affected patient, the rate of clearance of the phenylalanine from the blood is significantly low as compared to that of the normal and the heterozygote ones.
Pictorial representation:
Figure: The concentration of phenylalanine versus time graph.
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Chapter 18 Solutions
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