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Localization of the gene for congenital dyserythropoietic anemia type III, CDAN3, to chromosome 15q21-q25.
Umeå University, Faculty of Medicine, Department of Public Health and Clinical Medicine, Family Medicine.
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1995 (English)In: Human Molecular Genetics, ISSN 0964-6906, E-ISSN 1460-2083, Vol. 4, no 1, 109-12 p.Article in journal (Refereed) Published
Abstract [en]

Congenital dyserythropoietic anemia, type III (CDA III) is a rare autosomal dominant disorder characterized by macrocytic anemia, bone marrow erythroid hyperplasia and giant multinucleate erythroblasts. We have genetically characterized a large Swedish family in which the concurrence of CDA III and myeloma or benign monoclonal gammopathy is significantly higher than expected and have found that the causative genetic defect for CDA III maps to an 11 cM interval within 15q21-q25.

Place, publisher, year, edition, pages
1995. Vol. 4, no 1, 109-12 p.
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Medical and Health Sciences
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URN: urn:nbn:se:umu:diva-66827PubMedID: 7711721OAI: oai:DiVA.org:umu-66827DiVA: diva2:609411
Available from: 2013-03-05 Created: 2013-03-05 Last updated: 2017-12-06

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Sandström, Herbert

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