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 23, Problem 43P
Interpretation Introduction

Interpretation:

The possible explanation for the symptoms of pyruvate carboxylase deficiency disorder related to the biochemical pathways should be given.

Concept introduction:

Pyruvate carboxylase deficiency is also known as PC deficiency. It is a rare genetic disorder. It is present at birth that is considered by the failure to live. It shows some more symptoms such as recurrent seizures, developmental delay. It leads to the accumulation of lactic acid and other potentially toxic compounds in the blood.

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