Neuronopathic Types of Mucopolysaccharidoses: Pathogenesis and Emerging Treatments

• Główni autorzy: L. A. Osipova (Autor), L. M. Kuzenkova (Autor), L. S. Namazova-Baranova (Autor), A. K. Gevorkyan (Autor), T. V. Podkletnova (Autor), N. D. Vashakmadze (Autor)
• Format: Książka
• Wydane: "Paediatrician" Publishers LLC, 2015-11-01T00:00:00Z.
• Hasła przedmiotowe: article
• Dostęp online: Connect to this object online.

Mucopolysaccharidoses are a group of hereditary metabolic diseases, relating to lysosomal storage disorders and caused by a deficiencyof the enzymes, involved in degradation of glycosaminoglycans (mucopolysaccharides). Severe forms of mucopolysaccharidoses of types I, II and VII and mucopolysacchari...