Congenital dyserythropoietic anemia type II (CDAII/HEMPAS): Where are we now?
Author:
Publisher
Elsevier BV
Subject
Molecular Biology,Molecular Medicine
Reference58 articles.
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2. Localization of the gene for congenital dyserythropoietic anemia type I to a <1 cM interval on chromosome 15q15.1–15.3;Tamary;Am. J. Hum. Genet.,1998
3. Congenital dyserythropoietic anemia type I is caused by mutations in codanin-1;Dgany;Am. J. Hum. Genet.,2002
4. Congenital dyserythropoietic anemia type I (CDA I): molecular genetics, clinical appearance, and prognosis based on long-term observation;Heimpel;Blood,2006
5. Congenital dyserythropoietic anemia type III;Sandstrom;Haematologica,2000
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1. Using the Zebrafish as a Genetic Model to Study Erythropoiesis;International Journal of Molecular Sciences;2021-09-28
2. Congenital dyserythropoietic anemias;Blood;2020-09-10
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4. Inherited Bone Marrow Failure Syndromes;Anemia in the Young and Old;2018-11-14
5. CD44 as a Potential Screening Marker for Preliminary Differentiation Between Congenital Dyserythropoietic Anemia Type II and Hereditary Spherocytosis;Cytometry Part B: Clinical Cytometry;2016-11-23
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