Amanote Research
Register
Sign In
Congenital Dyserythropoietic Anemia Type III
doi 10.32388/4w26zi
Full Text
Open PDF
Abstract
Available in
full text
Date
February 10, 2020
Authors
Unknown
Publisher
Qeios
Related search
Thrombocytopenia With Congenital Dyserythropoietic Anemia
Codanin-1 Mutations in Congenital Dyserythropoietic Anemia Type 1 Affect HP1 Localization in Erythroblasts
Blood
Biochemistry
Immunology
Cell Biology
Hematology
Diagnosis: Congenital Dyserythropoietic Anemia Type 2 Due to Compound Heterozygote Mutation in SEC23B Gene
Turkish Journal of Haematology
Hematology
Glycophorin a in Two Patients With Congenital Dyserythropoietic Anemia Type I and Type II Is Partly Unglycosylated.
Acta Biochimica Polonica
Biochemistry
Genetics
Molecular Biology
Congenital Dyserythropoietic Anemia Type 1: A Case With Novel Compound Heterozygous Mutations in the C15orf41 Gene
American Journal of Hematology
Hematology
Bulky Extramedullary Hematopoiesis Is Not a Rare Complication of Congenital Dyserythropoietic Anemia
Annals of Hematology
Medicine
Hematology
Congenital Dyserythropoietic Anemia Associated to a GATA1 Mutation Aggravated by Pyruvate Kinase Deficiency
Annals of Hematology
Medicine
Hematology
Characterization of the Interactions Between Codanin-1 and C15Orf41, Two Proteins Implicated in Congenital Dyserythropoietic Anemia Type I Disease
BMC Molecular and Cell Biology
Cell Biology
Molecular Biology
Congenital Dyserythropoietic Anemia Type 1: Report of One Patient and Analysis of Previously Reported Patients Treated With Interferon Alpha
Indian Journal of Hematology and Blood Transfusion
Hematology
