ISSN: 1300-7777 E-ISSN: 1308-5263
Diagnosis: Congenital Dyserythropoietic Anemia Type 2 Due to Compound Heterozygote Mutation in SEC23B Gene [Turk J Hematol]
Turk J Hematol. 2015; 32(3): 283-284 | DOI: 10.4274/tjh.2014.0478  

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

Fatih Demircioğlu1, Mustafa Erkoçoğlu2, Mustafa Dilek2, Mervan Bekdaş2, Sevil Göksügür2, Semra Büyükkorkmaz2, Seher Açar2
1Abant İzzet Baysal University Faculty of Medicine, Department of Pediatrics, Division of Pediatric Hematology, Bolu, Turkey
2Abant İzzet Baysal University Faculty of Medicine, Department of Pediatrics, Bolu, Turkey

Keywords: Anemia, Congenital dyserythropoietic anemia type 2, SEC23B gene


Bileşik Heterozigot SEC23B Gen Mutasyonu Olan Konjenital Diseritropetik Anemi Tip 2 Olgusu

Fatih Demircioğlu1, Mustafa Erkoçoğlu2, Mustafa Dilek2, Mervan Bekdaş2, Sevil Göksügür2, Semra Büyükkorkmaz2, Seher Açar2
1Abant İzzet Baysal University Faculty of Medicine, Department of Pediatrics, Division of Pediatric Hematology, Bolu, Turkey
2Abant İzzet Baysal University Faculty of Medicine, Department of Pediatrics, Bolu, Turkey

Anahtar Kelimeler: Anemi, Konjenital diseritropetik anemi tip 2, SEC23B geni


Fatih Demircioğlu, Mustafa Erkoçoğlu, Mustafa Dilek, Mervan Bekdaş, Sevil Göksügür, Semra Büyükkorkmaz, Seher Açar. Diagnosis: Congenital Dyserythropoietic Anemia Type 2 Due to Compound Heterozygote Mutation in SEC23B Gene. Turk J Hematol. 2015; 32(3): 283-284

Corresponding Author: Fatih Demircioğlu, Türkiye


TOOLS
Full Text PDF
Print
Download citation
RIS
EndNote
BibTex
Medlars
Procite
Reference Manager
Share with email
Share
Send email to author

Similar articles
PubMed
Google Scholar


 



Impact Factor (2016) = 0.686