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
- EP ID EP95294
- DOI 10.4274/tjh.2014.0478
- Views 94
- Downloads 0
Clonal Evolution of Acute Myeloid Leukemia with CEBPA Double Mutations after Long-Term Remission: Case Report and a Literature Review
.
Light Chain Myeloma with Highly Atypical Plasma Cells and Extensive Auer Rod-Like Inclusions
.
Hb D-Los Angeles [beta121(GH4)Glu>Gln] and Hb Beograd [beta121(GH4)Glu>Val]: Implications for their laboratory diagnosis and genetic origins
Objective: The aim of this study was to determine the laboratory diagnosis and genetic origins of the hemoglobin (Hb) variants, Hb D-Los Angeles and Hb Beograd observed frequently in our region. Material and Methods: Hb...
Clinical Trials in Turkey
Turkey is an emerging economy in almost all sectors, and especially in pharmaceuticals. Turkey has had clinical trial legislation for a long time. There are also clinical trial regulations and guidelines. Turkey has take...
An Unusual Giant Leg Ulcer as a Rare Presentation of Sweet’s Syndrome in a Patient with Hairy Cell Leukemia Successfully Managed by Splenectomy
To the Editor,