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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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Xehetasun bibliografikoak
Argitaratua izan da:J Cell Mol Med
Egile Nagusiak: Talmaci, R., Traeger‐Synodinos, J., Kanavakis, E., Coriu, D., Colita, D., Gavrila, L.
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: Blackwell Publishing Ltd 2007
Gaiak:
Sarrera elektronikoa: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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