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

Journal Title: Turkish Journal of Hematology - Year 2015, Vol 32, Issue 3

Abstract

Authors and Affiliations

Fatih Demircioğlu, Mustafa Erkoçoğlu, Mervan Bekdaş, Sevil Göksügür, Semra Büyükkorkmaz, Seher Açar

Keywords

Related Articles

Glomerular and Tubular Functions in Children and Adults with Transfusion-Dependent Thalassemia

This study aimed at assessing renal functions in patients with transfusion-dependent thalassemia (TDT). Fifty patients and 30 controls were enrolled in this prospective study. Serum levels of electrolytes and albumin wer...

The Effect of Hyperparathyroid State on Platelet Functions and Bone Loss

Objective: Coagulation and fibrinolysis defects were reported in primary hyperparathyroid patients. However, there are not enough data regarding platelet functions in this group of patients. Our aim was to evaluate the p...

Download PDF file
  • EP ID EP95294
  • DOI 10.4274/tjh.2014.0478
  • Views 99
  • Downloads 0

How To Cite

Fatih Demircioğlu, Mustafa Erkoçoğlu, Mervan Bekdaş, Sevil Göksügür, Semra Büyükkorkmaz, Seher Açar (2015). Diagnosis: Congenital Dyserythropoietic Anemia Type 2 Due to Compound Heterozygote Mutation in SEC23B Gene. Turkish Journal of Hematology, 32(3), 283-284. https://europub.co.uk/articles/-A-95294