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A Swedish family with the rare Phe33Leu transthyretin mutation.
Umeå University, Faculty of Medicine, Department of Medical Biosciences, Medical and Clinical Genetics.
Umeå University, Faculty of Medicine, Department of Public Health and Clinical Medicine.ORCID iD: 0000-0002-3822-0725
Umeå University, Faculty of Medicine, Department of Public Health and Clinical Medicine.
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2005 (English)In: Amyloid, ISSN 1350-6129, Vol. 12, no 3, p. 189-92Article in journal (Refereed) Published
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2005. Vol. 12, no 3, p. 189-92
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URN: urn:nbn:se:umu:diva-14699DOI: doi:10.1080/13506120500221989PubMedID: 16194875OAI: oai:DiVA.org:umu-14699DiVA, id: diva2:154371
Available from: 2007-06-29 Created: 2007-06-29 Last updated: 2023-03-07Bibliographically approved

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Publisher's full textPubMedhttp://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Retrieve&list_uids=16194875&dopt=Citation

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Hellman, UrbanSuhr, Ole B

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Medical and Clinical GeneticsDepartment of Public Health and Clinical Medicine

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CiteExportLink to record
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