MUCOPOLYSACCHARIDOSIS TYPE II

MUCOPOLYSACCHARIDOSIS TYPE II

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Article is devoted to one of the orphan diseases — mucopolysaccharidosis (MPS), which is the result of any lysosomal enzyme deficiency (which determines the type of illness). The most common is the MPS type II (Hunter syndrome), developing as a result of deficiency of the enzyme alpha-L-iduronosulph...

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Bibliographic Details
Main Authors:	N.D. Vashakmadze, L.S. Namazova-Baranova, A.K. Gevorkyan, L.M. Kuzenkova, A.D. Khristochevskiy, L.M. Vysotskaya, A.S. Dadashev
Format:	Article
Language:	English
Published:	Paediatrician Publishers, LLC 2011-06-01
Series:	Pediatričeskaâ Farmakologiâ
Online Access:	https://pf.spr-journal.ru/jour/article/view/1273

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