Evidence of genetic heterogeneity in congenital dyserythropoietic anaemia type I
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2141.2006.06089.x/fullpdf
Reference6 articles.
1. Congenital Dyserythropoietic Anemia Type I Is Caused by Mutations in Codanin-1
2. Congenital dyserythropoietic anemia type I (CDA I): molecular genetics, clinical appearance, and prognosis based on long-term observation
3. Non-haematological traits associated with congenital dyserythropoietic anaemia type 1: a new entity emerging
4. Localization of the Gene for Congenital Dyserythropoietic Anemia Type I to a <1-cM Interval on Chromosome 15q15.1-15.3
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1. Diagnosis and management of congenital dyserythropoietic anemias;Expert Review of Hematology;2016-01-06
2. "Diabetes Associated Genes from the Dark Matter of the Human Proteome";MOJ Proteomics & Bioinformatics;2014-07-19
3. Homozygous mutations in a predicted endonuclease are a novel cause of congenital dyserythropoietic anemia type I;Haematologica;2013-05-28
4. Anémies dysérythropoïétiques congénitales;Hématologie;2010-05
5. Epidemiology of Rare Anaemias in Europe;Rare Diseases Epidemiology;2010
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