Biochemistry
Biochemistry
9th Edition
ISBN: 9781319114671
Author: Lubert Stryer, Jeremy M. Berg, John L. Tymoczko, Gregory J. Gatto Jr.
Publisher: W. H. Freeman
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Chapter 16, Problem 53P
Interpretation Introduction

Interpretation:

The people with galactosemia have central nervous system defects.

Concept introduction:

Galactosemia is a genetic disorder in which galactose sugar is not metabolized properly. Galactose is a part of lactose, which is found in all dairy products. So, galactose is some amount is present in the person’s diet. Galactosemia occurs due to the improper functioning of galactose-1-phosphate uridyl transferase (GALT) enzyme.

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