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

Turkish Journal of Haematology - Turkey
doi 10.4274/tjh.2014.0478
Full Text
Abstract

Available in full text

Categories
Hematology
Date
Authors
Publisher

Galenos Yayinevi

Related search

Congenital Dyserythropoietic Anemia Type III

2020English

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

American Journal of Hematology
Hematology
2018English

Congenital Dyserythropoietic Anemia Associated to a GATA1 Mutation Aggravated by Pyruvate Kinase Deficiency

Annals of Hematology
MedicineHematology
2016English

Thrombocytopenia With Congenital Dyserythropoietic Anemia

2020English

Congenital Myasthenic Syndrome Due to Mutation in CHRNE Gene

Child Neurology
2017English

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

Blood
BiochemistryImmunologyCell BiologyHematology
2011English

A Case of Congenital Dyserythropoietic Anemia Type 1 in a Japanese Adult With a CDAN1 Gene Mutation and an Inappropriately Low Serum Hepcidin-25 Level

Internal Medicine
Internal MedicineMedicine
2012English

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

Blood
BiochemistryImmunologyCell BiologyHematology
2008English

Congenital Central Hypothyroidism Due to a Homozygous Mutation in theTSHβSubunit Gene

Case Reports in Pediatrics
2011English

Amanote Research

Note-taking for researchers

Follow Amanote

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

Privacy PolicyRefund Policy