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[Mucopolysaccharidoses. New therapeutic possibilities increase the need of early diagnosis]
Uppsala University, Medicinska vetenskapsområdet, Faculty of Medicine, Department of Genetics and Pathology.
2002 (English)In: Lakartidningen, ISSN 0023-7205, Vol. 99, no 16, 1804-9 p.Article in journal (Other scientific) Published
Place, publisher, year, edition, pages
2002. Vol. 99, no 16, 1804-9 p.
Keyword [en]
Adolescent, Bone Marrow Transplantation, Child, English Abstract, Female, Humans, Incidence, Infant, Male, Mucopolysaccharidoses/diagnosis/epidemiology/genetics/*therapy, Mucopolysaccharidosis I/diagnosis/epidemiology/therapy, Mucopolysaccharidosis VI/diagnosis/epidemiology/therapy, Prenatal Diagnosis/methods, Prevalence, Social Support, Sweden/epidemiology
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URN: urn:nbn:se:uu:diva-73152PubMedID: 12043480OAI: oai:DiVA.org:uu-73152DiVA: diva2:101063
Available from: 2005-06-01 Created: 2005-06-01 Last updated: 2011-01-13

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Bondeson, Marie-Louise

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