Glycophorin a in Two Patients With Congenital Dyserythropoietic Anemia Type I and Type II Is Partly Unglycosylated.

Acta Biochimica Polonica - Poland
doi 10.18388/abp.2000_3995
Full Text
Abstract

Available in full text

Date
Authors
Publisher

Polskie Towarzystwo Biochemiczne (Polish Biochemical Society)

Related search

Congenital Dyserythropoietic Anemia Type III

2020English

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 BiologyMolecular Biology
2020English

Thrombocytopenia With Congenital Dyserythropoietic Anemia

2020English

Congenital Dyserythropoietic Anemia Type 1: A Case With Novel Compound Heterozygous Mutations in the C15orf41 Gene

American Journal of Hematology
Hematology
2018English

Codanin-1, the Protein Encoded by the Gene Mutated in Congenital Dyserythropoietic Anemia Type I (CDAN1), Is Cell Cycle Regulated

Blood
BiochemistryImmunologyCell BiologyHematology
2008English

Codanin-1 Mutations in Congenital Dyserythropoietic Anemia Type 1 Affect HP1 Localization in Erythroblasts

Blood
BiochemistryImmunologyCell BiologyHematology
2011English

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
2015English

Diagnosis: Congenital Dyserythropoietic Anemia Type 2 Due to Compound Heterozygote Mutation in SEC23B Gene

Turkish Journal of Haematology
Hematology
2015English

Bulky Extramedullary Hematopoiesis Is Not a Rare Complication of Congenital Dyserythropoietic Anemia

Annals of Hematology
MedicineHematology
2009English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2024 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy