Levels of Lyso GL-1 in Gaucher and Lyso GL-3 in Fabry patients from India: Diagnostic aids for these lysosomal storage disorders
Author:
Publisher
Elsevier BV
Subject
Biochemistry, medical,Clinical Biochemistry,Biochemistry,General Medicine
Reference34 articles.
1. Inborn Errors of Metabolism Involving Complex Molecules: Lysosomal and Peroxisomal Storage Diseases;Bellettato;Pediatr Clin North Am.,2018
2. Treatment of lysosomal storage disorders;Mehta;BMJ,2003
3. A Review of Gaucher Disease Pathophysiology, Clinical Presentation and Treatments;Stirnemann;Int J Mol Sci.,2017
4. Biochemical and molecular characterization of adult patients with type I Gaucher disease and carrier frequency analysis of Leu444Pro - a common Gaucher disease mutation in India;Sheth;BMC Med Genet.,2018
5. Gaucher disease: single gene molecular characterization of one-hundred Indian patients reveals novel variants and the most prevalent mutation;Sheth;BMC Med Genet.,2019
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