Lysosomal storage disease: aspartylglycosaminuria

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This volumes provides a comprehensive and up-to-date review of aspartylglycosaminuria (AGU), which is one of the most common lysosomal diseases worldwide. It gives an overview of the disease from its discovery and early history to the most recent developments. It also provides detailed reference material for clinical specialists and researchers working in the field of inborn errors of metabolism, in particular on lysosomal diseases.