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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Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Università Cattolica del Sacro Cuore 2014
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4235483/
https://www.ncbi.nlm.nih.gov/pubmed/25408857
http://dx.doi.org/10.4084/MJHID.2014.071

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4235483/
https://www.ncbi.nlm.nih.gov/pubmed/25408857
http://dx.doi.org/10.4084/MJHID.2014.071

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