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Identification of mutations in the CACNL1A3 gene in 13 families of Scandinavian origin with hypokalemic periodic paralysis and evidence for a founder effect in the Danish families.
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1997 (English)In: Am J Med Genet, Vol. 69, 102- p.Article in journal (Refereed) Published
Place, publisher, year, edition, pages
1997. Vol. 69, 102- p.
URN: urn:nbn:se:uu:diva-52143OAI: oai:DiVA.org:uu-52143DiVA: diva2:80052
Available from: 2008-10-17 Created: 2008-10-17 Last updated: 2011-01-15

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