Hospital Sant Joan de Déu Barcelona

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Hospital Sant Joan de Déu Barcelona

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26/09/2010
Publicaciones científicas
Introduction : Hunter syndrome, or mucopolysaccharidosis type II, is an inherited disease linked to the X chromosome that is caused by a deficit of the enzyme iduronate-2-sulfatase and its main symptoms affect the bones, neurological system and the viscera. In order to further our knowledge of its natural history, a registry containing data about patients' clinical histories was compiled. The...