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Congenital dyserythropoietic anemia type III and primary hemochromatosis; coexistence of mutations in KIF23 and HFE
Umeå University, Faculty of Medicine, Department of Radiation Sciences.
Umeå University, Faculty of Medicine, Department of Medical Biosciences, Medical and Clinical Genetics.
Umeå University, Faculty of Medicine, Department of Medical Biosciences, Medical and Clinical Genetics.
Umeå University, Faculty of Medicine, Department of Radiation Sciences.ORCID iD: 0000-0001-6402-0463
2015 (English)In: Haematologica, ISSN 0390-6078, E-ISSN 1592-8721, Vol. 100, p. 594-594Article in journal, Meeting abstract (Other academic) Published
Place, publisher, year, edition, pages
2015. Vol. 100, p. 594-594
National Category
Hematology
Identifiers
URN: urn:nbn:se:umu:diva-110214ISI: 000361204904023OAI: oai:DiVA.org:umu-110214DiVA, id: diva2:861372
Conference
20th Congress of European-Hematology-Association, JUN 11-14, 2015, Vienna, AUSTRIA
Note

Supplement: 1Meeting Abstract: E1481

Available from: 2015-10-16 Created: 2015-10-16 Last updated: 2021-12-07Bibliographically approved

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Liljeholm, MariaVikberg, Ann-LouiseGolovleva, IrinaWahlin, Anders

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