Mucopolysaccharidosis I, II, and VI: brief review and guidelines for treatment

dc.creatorGiugliani, Roberto
dc.creatorFederhen, Andressa
dc.creatorRojas, Maria Ver??nica Mu??oz
dc.creatorAcosta, Angelina Xavier
dc.creatorBonfim, Carmen
dc.creatorLouren??o, Charles Marques
dc.creatorPimentel, Helena
dc.date.accessioned2013-11-01T19:51:31Z
dc.date.accessioned2019-05-22T15:35:09Z
dc.date.available2013-11-01T19:51:31Z
dc.date.available2019-05-22T15:35:09Z
dc.date.created2013-11-01T19:51:31Z
dc.date.issued2010
dc.identifierGenetics and Molecular Biology
dc.identifierhttp://repositorio.ufba.br/ri/handle/ri/13505
dc.identifierv. 33, n. 4
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/2706970
dc.description.abstract
dc.languageen
dc.sourcehttp://dx.doi.org/10.1590/S1415-47572010005000093
dc.subjectMucopolisaccharidoses
dc.subjectHurler syndrome
dc.subjectHunter syndrome
dc.subjectMaroteaux-Lamy syndrome
dc.subjectEnzyme replacement therapy
dc.subjectTreatment guidelines
dc.titleMucopolysaccharidosis I, II, and VI: brief review and guidelines for treatment
dc.typeArtigo de Peri??dico


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