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Congenital dyserythropoietic "anemia," type I
- ... Condition CDA-I CDA1 CDAI CDAN1_HUMAN codanin congenital dyserythropoietic anemia, type I DLT PRO1295 Tests of CDAN1 PubMed CODANIN ... of the CDAN1 gene reveals genetic heterogeneity in congenital dyserythropoietic anemia type I. Blood. 2006 Jun 15;107(12):4968- ...
- ... TYPE Ia; CDAN1A PubMed Denecke J, Marquardt T. Congenital dyserythropoietic anemia type II (CDAII/HEMPAS): where are we now? Biochim ... Olender T, Lancet D, Beckmann JS, Tamary H. Congenital dyserythropoietic anemia type I is caused by mutations in codanin-1. ...
- ... SEC23B NCBI Gene ClinVar Denecke J, Marquardt T. Congenital dyserythropoietic anemia type II (CDAII/HEMPAS): where are we now? Biochim ... affecting the secretory COPII coat component SEC23B cause congenital dyserythropoietic anemia type II. Nat Genet. 2009 Aug;41(8):936- ...
- ... of Majeed syndrome is a blood disorder called congenital dyserythropoietic anemia. This disorder is one of many types of anemia, all of which involve a shortage ...
- ... A main feature of this condition is a type of anemia called dyserythropoietic anemia, which is characterized by a shortage of ... blood cells, leading to anemia. The severity of dyserythropoietic anemia and thrombocytopenia can usually be predicted by the type of GATA1 gene mutation.When the two blood ...