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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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Dettagli Bibliografici
Pubblicato in:J Cell Mol Med
Autori principali: Talmaci, R., Traeger‐Synodinos, J., Kanavakis, E., Coriu, D., Colita, D., Gavrila, L.
Natura: Artigo
Lingua:Inglês
Pubblicazione: Blackwell Publishing Ltd 2007
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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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