Therapies for lysosomal storage diseases: Principles, practice, and prospects for refinements based on evolving

Gregory A Grabowski1, Pramod K Mistry2

  • 1University of Cincinnati College of Medicine, Department of Pediatrics, Department of Molecular Genetics, Biochemistry and Microbiology, United States of America; Division of Human Genetics, Cincinnati Children's Hospital Research Foundation, Cincinnati, OH, United States of America.

Abstract

No abstract available in PubMed .

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