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.
Reihe
Sprache
Verlagsort
Verlagsgruppe
Zielgruppe
Für höhere Schule und Studium
Für Beruf und Forschung
Illustrationen
50 s/w Abbildungen, 11 s/w Tabellen
60 figures, 8 tables
Gewicht
ISBN-13
978-3-540-62899-6 (9783540628996)
Schweitzer Klassifikation