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Common origin of the Val30Met mutation responsible for the amyloidogenic transthyretin type of familial amyloidotic polyneuropathy.
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2004 (English)In: Journal of medical genetics, ISSN 1468-6244, Vol. 41, no 4, e51- p.Article in journal (Refereed) Published
Place, publisher, year, edition, pages
2004. Vol. 41, no 4, e51- p.
Keyword [en]
Amino Acid Substitution, Amyloid/*genetics, Amyloid Neuropathies; Familial/*genetics, Europe, Founder Effect, Gene Frequency, Haplotypes, Humans, Japan, Microsatellite Repeats, Mutation; Missense, Polymorphism; Single Nucleotide, Prealbumin/*genetics
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URN: urn:nbn:se:umu:diva-13120PubMedID: 15060127OAI: oai:DiVA.org:umu-13120DiVA: diva2:152791
Available from: 2008-01-10 Created: 2008-01-10 Last updated: 2012-06-21Bibliographically approved

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Suhr, Ole B
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