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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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Detalhes bibliográficos
Publicado no:J Cell Mol Med
Main Authors: Talmaci, R., Traeger‐Synodinos, J., Kanavakis, E., Coriu, D., Colita, D., Gavrila, L.
Formato: Artigo
Idioma:Inglês
Publicado em: Blackwell Publishing Ltd 2007
Assuntos:
Acesso em linha: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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