This lysosomal storage disease is treated by reducing complex sphingolipid accumulation with the glucosylceramide synthase inhibiter miglustat. O Type 1 diabetes Gaucher disease Krabbe disease Fabry disease

This lysosomal storage disease is treated by reducing complex sphingolipid accumulation with the glucosylceramide synthase inhibiter miglustat. O Type 1 diabetes Gaucher disease Krabbe disease Fabry disease

Biochemistry

6th Edition

ISBN:9781305577206

Author:Reginald H. Garrett, Charles M. Grisham

Publisher:Reginald H. Garrett, Charles M. Grisham

Chapter18: Glycolysis

Section: Chapter Questions

Problem 20P: Understanding the Mechanism of Hemolytic Anemia Genetic defects in glycolytic enzymes can have...

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Q10: What is the correct answer option, pick one of the choices

This lysosomal storage disease is treated by reducing complex sphingolipid accumulation
with the glucosylceramide synthase inhibiter miglustat.
O Type 1 diabetes
Gaucher disease
Krabbe disease
Fabry disease

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