E-ISSN: 1308-5263
Two Rare Pathogenic HBB Variants in a Patient with β-Thalassemia Intermedia [Turk J Hematol]
Turk J Hematol. 2020; 37(2): 135-136 | DOI: 10.4274/tjh.galenos.2020.2020.0020  

Two Rare Pathogenic HBB Variants in a Patient with β-Thalassemia Intermedia

Veysel Sabri Hançer1, Tunç Fışgın2, Murat Büyükdoğan3
1İstinye University Faculty of Medicine, Department of Medical Biology, İstanbul, Turkey
2Altınbaş University Faculty of Medicine, Department of Pediatrics, İstanbul, Turkey
3İstinye University Faculty of Medicine, Department of Medical Genetics, İstanbul, Turkey

Keywords: Beta thalassemia, HBB, Variation


Bir Beta Talasemi İntermedya Hastasında İki Nadir Patojenik HBB Varyantı

Veysel Sabri Hançer1, Tunç Fışgın2, Murat Büyükdoğan3
1İstinye University Faculty of Medicine, Department of Medical Biology, İstanbul, Turkey
2Altınbaş University Faculty of Medicine, Department of Pediatrics, İstanbul, Turkey
3İstinye University Faculty of Medicine, Department of Medical Genetics, İstanbul, Turkey

Anahtar Kelimeler: Beta talasemi, HBB, Varyasyon


Veysel Sabri Hançer, Tunç Fışgın, Murat Büyükdoğan. Two Rare Pathogenic HBB Variants in a Patient with β-Thalassemia Intermedia. Turk J Hematol. 2020; 37(2): 135-136

Corresponding Author: Veysel Sabri Hançer


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


Similar articles
PubMed
Google Scholar


 



Impact Factor (2018) = 0.779