Localization of the gene for congenital dyserythropoietic anemia type III, CDAN3, to chromosome 15q21-q25
Lind, Lisbet ; Sandström, Herbert ; Wahlin, Anders ; Eriksson, Mikael LU
; Nilsson-Sojka, Birgitta
; Sikström, Carin
and Holmgren, Gösta
(1995)
In Human Molecular Genetics
4(1).
p.109-112
- 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.
Please use this url to cite or link to this publication:
https://lup.lub.lu.se/record/cf9708f9-ec01-40dc-96a4-f7716a95fb99
- author
- Lind, Lisbet
; Sandström, Herbert
; Wahlin, Anders
; Eriksson, Mikael
LU
; Nilsson-Sojka, Birgitta
; Sikström, Carin
and Holmgren, Gösta
- publishing date
- 1995-01-01
- type
- Contribution to journal
- publication status
- published
- in
- Human Molecular Genetics
- volume
- 4
- issue
- 1
- pages
- 109 - 112
- publisher
- Oxford University Press
- external identifiers
-
- pmid:7711721
- scopus:0028869553
- ISSN
- 0964-6906
- DOI
- 10.1093/hmg/4.1.109
- language
- English
- LU publication?
- no
- id
- cf9708f9-ec01-40dc-96a4-f7716a95fb99
- date added to LUP
- 2020-02-18 17:12:54
- date last changed
- 2024-01-02 05:47:29
@article{cf9708f9-ec01-40dc-96a4-f7716a95fb99,
abstract = {{<p>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.</p>}},
author = {{Lind, Lisbet and Sandström, Herbert and Wahlin, Anders and Eriksson, Mikael and Nilsson-Sojka, Birgitta and Sikström, Carin and Holmgren, Gösta}},
issn = {{0964-6906}},
language = {{eng}},
month = {{01}},
number = {{1}},
pages = {{109--112}},
publisher = {{Oxford University Press}},
series = {{Human Molecular Genetics}},
title = {{Localization of the gene for congenital dyserythropoietic anemia type III, CDAN3, to chromosome 15q21-q25}},
url = {{http://dx.doi.org/10.1093/hmg/4.1.109}},
doi = {{10.1093/hmg/4.1.109}},
volume = {{4}},
year = {{1995}},
}