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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...
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| Autors principals: | , , , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Informa Healthcare
2013
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3667679/ https://ncbi.nlm.nih.gov/pubmed/23614625 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3109/03630269.2013.775149 |
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