MUCOPOLYSACCHARIDOSIS TYPE II
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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| Autors principals: | , , , , , , |
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| Format: | Artigo |
| Idioma: | Russo |
| Publicat: |
Union of pediatricians of Russia
2011-06-01
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| Col·lecció: | Педиатрическая фармакология |
| Accés en línia: | https://www.pedpharma.ru/jour/article/view/1273 |
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