The Evaluation of Skeletal Manifestations in Patients with Gaucher Disease
Aim:Gaucher disease (GD) is the most prevalent hereditary lysosomal storage disorder, affecting multiple organ systems. It is characterized by a deficiency of the enzyme glucocerebrosidase leading to an accumulation of glucosylceramide in lysosomes. The majority of patients present with hepatospleno...
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| Main Authors: | , , , , |
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| Format: | Book |
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Galenos Yayinevi,
2021-09-01T00:00:00Z.
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| Call Number: |
A1234.567 |
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| Copy 1 | Available |