Spectrum of Beta Globin Gene Mutations in Egyptian Children with β-Thalassemia

BACKGROUND: The molecular defects resulting in a β-thalassemia phenotype, in the Egyptian population, show a clear heterogenic mutations pattern. PCR-based techniques, including direct DNA sequencing are effective on the molecular detection and characterization of these mutations. The molecular char...

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Опубликовано в: :Mediterr J Hematol Infect Dis
Главные авторы: El-Shanshory, MR, Hagag, AA, Shebl, SS, Badria, IM, Abd Elhameed, AH, Abd El-Bar, ES, Al-Tonbary, Y, Mansour, A, Hassab, H, Hamdy, M, Alfy, M, Sherief, L, Sharaf, E
Формат: Artigo
Язык:Inglês
Опубликовано: Università Cattolica del Sacro Cuore 2014
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Original Article
Online-ссылка:https://ncbi.nlm.nih.gov/pmc/articles/PMC4235483/
https://ncbi.nlm.nih.gov/pubmed/25408857
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4084/MJHID.2014.071
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