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Interaction of Hb Adana (HBA2: c.179G>A) with Deletional and Nondeletional α (+)-Thalassemia Mutations: Diverse Hematological and Clinical Features
We describe 27 cases of mild-to-severe α-thalassemia (α-thal) syndrome caused by interaction of Hb Adana [α59(E8)Gly→Asp, GGC>GAC (α2)] with deletional and nondeletional α(+)-thal mutations in Indonesian patients. Hematological profiles and clinical manifestations of all patients were assessed by...
| Autores principales: | , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Informa Healthcare
2013
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3667679/ https://www.ncbi.nlm.nih.gov/pubmed/23614625 http://dx.doi.org/10.3109/03630269.2013.775149 |