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Coinheritance of Sicilian (δβ)(0)-Thalassemia and Two Rare Hemoglobin Variants: A Complex Case of Hemoglobinopathy
α-Thalassemia (α-thal) is considered as the most common inherited hemoglobin disorder worldwide. The present study describes the first observation of a combination of rare α-chain variants, and β-globin gene cluster deletion. A 21-year-old woman with thalassemia trait, marked microcytosis, mild anem...
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| Publicado en: | Indian J Clin Biochem |
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| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Springer India
2017
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5891461/ https://ncbi.nlm.nih.gov/pubmed/29651217 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s12291-017-0676-z |
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