Localization of the gene for congenital dyserythropoietic anemia type III, CDAN3, to chromosome 15q21-q25
- 1 January 1995
- journal article
- research article
- Published by Oxford University Press (OUP) in Human Molecular Genetics
- Vol. 4 (1) , 109-112
- https://doi.org/10.1093/hmg/4.1.109
Abstract
Congential dyserythropoietic anemia, type III (CDA III) is a rare autosomal dominant disorder characterized by macrocytic anemia, bone marrow erythroid hyperplasia and giant multlnucleate 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.Keywords
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