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Turkish Journal of Hematology
(Jul 2015)
Diagnosis: Congenital Dyserythropoietic Anemia Type 2 Due to Compound Heterozygote Mutation in SEC23B Gene
Fatih Demircioğlu,
Mustafa Erkoçoğlu,
Mustafa Dilek,
Mervan Bekdaş,
Sevil Göksügür,
Semra Büyükkorkmaz,
Seher Açar
Affiliations
Fatih Demircioğlu
Abant İzzet Baysal University Faculty of Medicine, Department of Pediatrics, Division of Pediatric Hematology, Bolu, Turkey
Mustafa Erkoçoğlu
Abant İzzet Baysal University Faculty of Medicine, Department of Pediatrics, Bolu, Turkey
Mustafa Dilek
Abant İzzet Baysal University Faculty of Medicine, Department of Pediatrics, Bolu, Turkey
Mervan Bekdaş
Abant İzzet Baysal University Faculty of Medicine, Department of Pediatrics, Bolu, Turkey
Sevil Göksügür
Abant İzzet Baysal University Faculty of Medicine, Department of Pediatrics, Bolu, Turkey
Semra Büyükkorkmaz
Abant İzzet Baysal University Faculty of Medicine, Department of Pediatrics, Bolu, Turkey
Seher Açar
Abant İzzet Baysal University Faculty of Medicine, Department of Pediatrics, Bolu, Turkey
DOI
https://doi.org/10.4274/tjh.2014.0478
Journal volume & issue
Vol. 32, no. 3
pp. 283 – 284
Abstract
Read online
No abstracts available.
Keywords
anemia
congenital dyserythropoietic anemia type 2
sec23b gene
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