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Molecular Genetic Characterization of β-Thalassemia and Sickle Cell Syndrome in the Albanian Population

β-Thalassemia (β-thal) is a major public health problem in Albania as it is in many Mediterranean countries. We determined the different β-thal alleles that are present in the Albanian population by using the temporal temperature gradient electrophoresis (TTGE) method because of its high throughput,...

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Detalhes bibliográficos
Main Authors: Babameto-Laku, A, Mitre, A, Berisha, S, Mokini, V, Roko, D
Formato: Artigo
Idioma:Inglês
Publicado em: Macedonian Science of Sciences and Arts 2011
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3776692/
https://ncbi.nlm.nih.gov/pubmed/24052702
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2478/v10034-011-0017-0
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