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Scanning of β‐globin gene for identification of β‐thalassemia mutation in Romanian population
β‐Thalassemia is uncommon (0.5%) in the Romanian population, but it must be considered in the differential diagnosis of hypochromic anemia. The molecular characterization of β‐thalassemia is absolutely necessary for molecular diagnosis, as well as any genetic epidermiological study in this region. M...
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| Pubblicato in: | J Cell Mol Med |
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| Autori principali: | , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Blackwell Publishing Ltd
2007
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6740280/ https://ncbi.nlm.nih.gov/pubmed/15256071 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1582-4934.2004.tb00278.x |
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