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July 3, 2024Hemoglobin

Dominant Beta Thalassemia: A Very Rare Cause of Thalassemia in a Mediterranean Country

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ÇCÇağrı CoşkunHacettepe UniversityŞÜŞule ÜnalHacettepe University Hospital

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Cite This Study

Coşkun et al. (2024) studied this question.

synapsesocial.com/papers/68e61810b6db6435875aaed2https://doi.org/10.1080/03630269.2024.2386067
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Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Distinct Distribution of HBB Variants in Two Cohorts of Beta Thalassemia Patients, and a Novel Variant from Turkey2024
  2. 2Alpha thalassemia in Istanbul: Distribution of deletions in alpha-globin gene cluster2024 · 1 citations
  3. 3Clinical and hematological characteristics of beta-plus thalassemia and uncommon beta-chain hemoglobin variants in Northern Thailand2025
  4. 4Genetic Study for Identifying Beta Thalassemia Trait in Relatives of Children with Beta Thalassemia Major2024
  5. 5Severe Transfusion-Dependent Thalassemia in Compound Heterozygote Palestinian Siblings with Two α-Globin Gene Defects, Hb Taybe D <i>HBA1</i> : C.119_121delCCA Mutation and <i>HBA2</i> : C.*94A &gt; G Mutation2024