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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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Bibliografische gegevens
Gepubliceerd in:J Cell Mol Med
Hoofdauteurs: Talmaci, R., Traeger‐Synodinos, J., Kanavakis, E., Coriu, D., Colita, D., Gavrila, L.
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: Blackwell Publishing Ltd 2007
Onderwerpen:
Online toegang: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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