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AB111. HBB: c. -78A>G/nt-28(A>G) associated with Cd 26(A-G) HbE, beta thalassemia variant causes thalassemia intermedia
β-thalassemia is the most common single gene disorder worldwide and in Vietnam. In the present study we report in members of a family from North Vietnam, the mother compound heterozygous thalassemia intermedia presenting mutation of hemoglobin HBB: c. -78A>G/nt-28(A>G) with Cd 26(A-G) HbE. The...
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| Publicado no: | Ann Transl Med |
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| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
AME Publishing Company
2015
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4563490/ https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3978/j.issn.2305-5839.2015.AB111 |
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