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Lafora progressive myoclonus epilepsy: disease course homogeneity in a genetic isolate.
Uppsala University, Medicinska vetenskapsområdet, Faculty of Medicine, Department of Genetics and Pathology.
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2008 (English)In: J Child Neurol, ISSN 0883-0738, Vol. 23, no 2, 240-2 p.Article in journal (Refereed) Published
Place, publisher, year, edition, pages
2008. Vol. 23, no 2, 240-2 p.
Keyword [en]
Adolescent, Adult, Age of Onset, Carrier Proteins/*genetics/metabolism, Consanguinity, DNA Mutational Analysis, Death, Humans, Lafora Disease/ethnology/*genetics/mortality/physiopathology, Oman, Population Groups/*genetics, Skin/metabolism
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URN: urn:nbn:se:uu:diva-16141PubMedID: 18263761OAI: oai:DiVA.org:uu-16141DiVA: diva2:43912
Available from: 2008-04-30 Created: 2008-04-30 Last updated: 2011-01-11

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