Compare the complex lipid structures listed for the lipid storage diseases with missing or defective enzymes. Explain why the missing enzyme in Fabry’s disease is alpha-galactosidase and not beta-galactosidase. Concept Introduction: Fabry’s disease is the result of the mutation of the gene responsible for making alpha-galactosidase enzyme.

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Answer 1

Question

Chapter 21, Problem 21.56P

Interpretation Introduction

Interpretation:

Compare the complex lipid structures listed for the lipid storage diseases with missing or defective enzymes. Explain why the missing enzyme in Fabry’s disease is alpha-galactosidase and not beta-galactosidase.

Concept Introduction:

Fabry’s disease is the result of the mutation of the gene responsible for making alpha-galactosidase enzyme.

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Answer 2

Question

Chapter 21, Problem 21.56P

Interpretation Introduction

Interpretation:

Compare the complex lipid structures listed for the lipid storage diseases with missing or defective enzymes. Explain why the missing enzyme in Fabry’s disease is alpha-galactosidase and not beta-galactosidase.

Concept Introduction:

Fabry’s disease is the result of the mutation of the gene responsible for making alpha-galactosidase enzyme.

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Answer 3

Question

Chapter 21, Problem 21.56P

Interpretation Introduction

Interpretation:

Compare the complex lipid structures listed for the lipid storage diseases with missing or defective enzymes. Explain why the missing enzyme in Fabry’s disease is alpha-galactosidase and not beta-galactosidase.

Concept Introduction:

Fabry’s disease is the result of the mutation of the gene responsible for making alpha-galactosidase enzyme.

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Answer 4

Question

Chapter 21, Problem 21.56P

Interpretation Introduction

Interpretation:

Compare the complex lipid structures listed for the lipid storage diseases with missing or defective enzymes. Explain why the missing enzyme in Fabry’s disease is alpha-galactosidase and not beta-galactosidase.

Concept Introduction:

Fabry’s disease is the result of the mutation of the gene responsible for making alpha-galactosidase enzyme.

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Answer 5

Chapter 21, Problem 21.56P

Interpretation Introduction

Interpretation:

Compare the complex lipid structures listed for the lipid storage diseases with missing or defective enzymes. Explain why the missing enzyme in Fabry’s disease is alpha-galactosidase and not beta-galactosidase.

Concept Introduction:

Fabry’s disease is the result of the mutation of the gene responsible for making alpha-galactosidase enzyme.

Answer 6

Chapter 21, Problem 21.56P

Interpretation Introduction

Interpretation:

Compare the complex lipid structures listed for the lipid storage diseases with missing or defective enzymes. Explain why the missing enzyme in Fabry’s disease is alpha-galactosidase and not beta-galactosidase.

Concept Introduction:

Fabry’s disease is the result of the mutation of the gene responsible for making alpha-galactosidase enzyme.

Answer 7

Chapter 21, Problem 21.56P

Interpretation Introduction

Interpretation:

Compare the complex lipid structures listed for the lipid storage diseases with missing or defective enzymes. Explain why the missing enzyme in Fabry’s disease is alpha-galactosidase and not beta-galactosidase.

Concept Introduction:

Fabry’s disease is the result of the mutation of the gene responsible for making alpha-galactosidase enzyme.

Answer 8

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Answer 9

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Answer 10

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Answer 11

Ch. 21.8 - Prob. 21.1P Ch. 21 - 21-2 Why are fats a good source of energy for...Ch. 21 - 21-3 Proteins, nucleic acids, and carbohydrates...Ch. 21 - Prob. 21.4P Ch. 21 - Prob. 21.5P Ch. 21 - Prob. 21.6P Ch. 21 - 21-7 For the diglycerides in Problem 21-6, predict...Ch. 21 - 21-8 Predict which acid in each pair has the...Ch. 21 - Prob. 21.9P Ch. 21 - Prob. 21.10P

Solution Summary: The author explains that Fabry's disease is the result of a mutation of the gene responsible for making alpha-galactosidase enzyme, located on the X-chromosome.

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Chapter 21 Solutions