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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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Podrobná bibliografie
Vydáno v:J Cell Mol Med
Hlavní autoři: Talmaci, R., Traeger‐Synodinos, J., Kanavakis, E., Coriu, D., Colita, D., Gavrila, L.
Médium: Artigo
Jazyk:Inglês
Vydáno: Blackwell Publishing Ltd 2007
Témata:
On-line přístup: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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