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Heterozygous Beta Chain Variant Hemoglobin Pusan: A Rare Case Report in Turkish Population
The case, detected during routine thalassemia (hemoglobin variant) screening, was a 25-year-old male patient of Turkish origin. Physical examination revealed no abnormal findings. Laboratory findings did not reveal any signs of anemia (iron deficiency, B12 deficiency, etc.). However, when the hemogl...
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| Publicado no: | Medeni Med J |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Istanbul Medeniyet University
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7433718/ https://ncbi.nlm.nih.gov/pubmed/32821467 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5222/MMJ.2019.10476 |
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